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Therapy System

User Manual
Operation & Installation
Instructions for:
Color Series
2765CS- Two Channel
Electrotherapy System
2762CC- Two Channel
Combination System

Monochromatic Series
2773MS- Two Channel
Electrotherapy System
2772MC- Two Channel
Combination System

Optional Modules
2005 Encore Medical, L.P.

2770- Channel 3/4


Electrotherapy Module

TABLE OF CONTENTS

Intelect Advanced Therapy System

FOREWORD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
PRODUCT DESCRIPTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
SAFETY PRECAUTIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
PRECAUTIONARY DEFINITIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
CAUTIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
WARNINGS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
DANGERS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
ELECTROTHERAPY INDICATIONS, CONTRAINDICATIONS, AND
ADVERSE EFFECTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Indications for VMS, VMS Burst, Russian, TENS, High Voltage Pulsed . . . . .
Current (HVPC), Interferential, and Premodulated waveforms. . . . . . . . . . . 7
Additional Indications for Microcurrent, Interferential, Premodulated, . .
VMS, VMS Burst, and TENS waveforms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Indications for Galvanic Continuous Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Additional Precautions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Adverse Eects. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
ULTRASOUND INDICATIONS AND CONTRAINDICATIONS . . . . . . . . . . . 9
Indications for Ultrasound . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Additional Precautions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
NOMENCLATURE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1014
INTELECT ADVANCED ELECTROTHERAPY AND COMBINATION
THERAPY SYSTEMS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Two (2) Channel Electrotherapy System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Two (2) Channel Combination System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Front Access Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Rear Access Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
USER INTERFACE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
SYMBOL DEFINITIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
System Hardware Symbols. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
SystemSoftware Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Operator Remote . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Battery Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Channel 3/4ElectrothrapyModule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13

GENERAL TERMINOLOGY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1526
SYSTEM SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
DIMENSIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Width. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Standard Weight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Power (Combination and Electrotherapy Units) . . . . . . . . . . . . . . . . . . . . . . . . . 15
Electrical Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
WAVEFORM SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
IFC (Interferential) Traditional (4 Pole) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
TENS- Asymmetrical Biphasic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
TENS- Symmetrical Biphasic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
TENS- Alternating Rectangular . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
TENS- Monophasic Rectangular . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
High Voltage Pulsed Current (HVPC). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
VMSTM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Diadynamic Waveforms. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
IFC Premodulated (2p) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Russian . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Microcurrent . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
VMSTM Burst . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
MONOPHASIC: Monophasic Rectangular Pulsed . . . . . . . . . . . . . . . . . . . . . . . . 22
MONOPHASIC: Monophasic Triangular Pulsed . . . . . . . . . . . . . . . . . . . . . . . . . . 22
GALVANIC: Continuous . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
GALVANIC: Interrupted . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Trbert (Ultrareiz) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
SURGED: Monophasic Rectangular . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
SURGED: Monophasic Triangular . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
ULTRASOUND SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Ultrasound . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
SETUP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2734
INTELECT ADVANCED COLOR SERIES THERAPY SYSTEMS. . . . . . . . . . 27
Color Series Standard Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Color Series Optional Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Mains Power Cords. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27

TABLE OF CONTENTS

Intelect Advanced Therapy System

INTELECT ADVANCED MONOCHROMATIC SERIES


THERAPY SYSTEMS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Monochromatic Series Standard Features. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Monochromatic Series Optional Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Mains Power Cords. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
THERAPY SYSTEM SET UP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Clinic Name . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Restore Default Protocols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Restore Default Unit Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Erase Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Set Date and Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Setting System Volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Ultrasound Coupling. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Display Unit Version Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Pad Contact Quality. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Select Language . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Connecting Accessories to the Therapy System . . . . . . . . . . . . . . . . . . . . . . . . . 34
PATIENT PREPARATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3539
ELECTROTHERAPY PATIENT PREPARATION. . . . . . . . . . . . . . . . . . . . . . . . . 35
Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Dura-Stick Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Reusable Carbon Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Dura-Stick Electrode Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Connecting Lead Wires. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Securing Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Reusable Carbon Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Connecting Lead Wires. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Conductive Medium . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Securing Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
ULTRASOUND PATIENT PREPARATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Preparing Treatment Area . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Size of Applicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Applicator Preparation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Conductive Medium . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Treatment Area. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39

Applicator Coupling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
OPERATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4094
OPERATOR INTERFACE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
HOME SCREEN. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
ELECTROTHERAPY SCREEN . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
GENERAL ELECTROTHERAPY WAVEFORM SET UP . . . . . . . . . . . . . . . . . . 43
Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Select Modality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Select Waveform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
View Waveform Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
View Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Edit Waveform Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Install Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Set Waveform Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Save to Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
ADJUSTING ELECTROTHERAPY CHANNEL PARAMETERS
DURING TREATMENT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
Select Channel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
Edit Channel Paramenters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
ULTRASOUND . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
Select Modality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
View Parameter Rationale . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
Sound Head Recommendation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
Edit Ultrasound Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
Head Warming . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
Set Ultrasound Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50

ii

TABLE OF CONTENTS

Intelect Advanced Therapy System

Save to Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50


Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
Editing Ultrasound from Home Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Editing Ultrasound from Treatment Review Screen . . . . . . . . . . . . . . . . . . . . . 51
QUICK LINK INDICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
Available Quick Link Indications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
Select Quick Link Indication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
View Waveform Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
View Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
Edit Waveform Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
Install Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Setting Waveform Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
Editing Parameters during Treatment Session . . . . . . . . . . . . . . . . . . . . . . . . . . 56
Save to Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
COMBINATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
Select Modality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
View Application Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
View Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
Access Combination Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
Edit Ultrasound Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
Select Waveform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
Edit Waveform Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
Set Waveform Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
Set Ultrasound Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60

Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
Save to Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
ADJUSTING COMBINATION PARAMETERS DURING TREATMENT . . . 62
Edit Waveform Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
Edit Ultrasound Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
PATIENT DATA CARD SET UP OF NEW CARD. . . . . . . . . . . . . . . . . . . . . . . . 63
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
Insert New Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
Setup Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
Set Up of New Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
Enter Patient ID . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64
Access Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
Electrode Placement Set Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
Access Pain Map. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66
Select Pain Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66
Add Pain Locations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66
Select Location of Pain . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67
Editing Pain Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67
Deleting Pain Locations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68
Pain Scales . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68
Select Pain Scale . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68
Adjust Pain Scale . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68
Save to Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69
EXISTING PATIENT DATA CARD USE. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70
Insert Existing Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70
Access Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70
View Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70
Starting a New Treatment from Patient Data Card . . . . . . . . . . . . . . . . . . . . . . 71
Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71
Set Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71
Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71
Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72
Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72

iii

TABLE OF CONTENTS

Intelect Advanced Therapy System

Erasing Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72


Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72
CLINICAL RESOURCES LIBRARY CLINICAL PROTOCOLS . . . . . . . . . . 73
Clinical Protocols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
Access Clinical Resources . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
Access Clinical Protocols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
Select Body Area . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
Select Clinical Indication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
Select Pathological Condition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
Select Pathological Severity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
View Waveform Rationale. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
View Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
Edit Modality Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Set Modality Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
Save to Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
CLINICAL RESOURCES LIBRARY CREATING USER PROTOCOLS . . . . 78
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
Select Modality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
Edit Modality Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
Select Clinical Resources Library. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
Enter User Protocol Name. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
CLINICAL RESOURCES LIBRARY DELETING USER PROTOCOLS . . . . 80
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80
Select Clinical Resources Library. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80
Select User Protocol to Delete . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80
Delete User Protocol . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80
CLINICAL RESOURCES LIBRARY USING USER PROTOCOLS . . . . . . . . 81
Access User Protocols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81
Select User Protocol. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81

View Waveform Rationale. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81


View Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82
Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82
Edit Modality Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82
Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82
Set Modality Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83
Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83
Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83
Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
Save to Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
CLINICAL RESOURCES LIBRARY CREATING NEW SEQUENCES . . . . . 85
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85
Access Sequencing. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85
Select Sequence. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85
Select First Waveform or Current . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85
Edit First Waveform or Current. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 86
Select Second Waveform or Current . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 86
Saving New Sequence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 86
Enter Sequence Name . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87
CLINICAL RESOURCES LIBRARY DELETING SEQUENCES . . . . . . . . . . . 88
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88
Access Sequencing. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88
Select Sequence. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88
Delete Sequence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88
CLINICAL RESOURCES LIBRARY USING SEQUENCES . . . . . . . . . . . . . . . 89
Access Sequencing. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89
Select Sequence. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89
Select Waveform/Current . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89
View Waveform Rationale. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
View Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
Set Sequence Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91

iv

TABLE OF CONTENTS

Intelect Advanced Therapy System

Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92
Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92
Save to Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92
Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92
CLINICAL RESOURCES LIBRARY MMC GRAPHICAL LIBRARY . . . . . . 93
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
Select Clinincal Resources Library . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
Select MMC Graphical Library . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
Select Body Area . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
Select Library Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 94
INSTALLATION/REMOVAL . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 95106
INSTALLATION CHANNEL 3/4 ELECTROTHERAPY MODULE . . . . . . . . 95
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 95
Nomenclature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 96
Specications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 97
Waveform & Current Specications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 97
Disconnect Mains Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 98
Remove Lead Wires and Accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 98
Remove Therapy System from Cart . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 98
Release Ribbon Cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99
Position Therapy System and Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99
Connect Ribbon Cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99
Set Therapy System onto Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .100
Secure Therapy System to Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .100
Front Access Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .100
Install Lead Wires and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .101
Install Front Access Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .101
Mount to Therapy System Cart . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .101
Connect Mains Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .101
Turn Therapy System On . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .102
REMOVAL CHANNEL 3/4 ELECTROTHERAPY MODULE . . . . . . . . . . . . 103
Disconnect Mains Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .103
Remove Therapy System from Cart . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .103
Remove Lead Wires and Accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .103
Remove Screws Securing Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .104

Disconnect Ribbon Cable at Module. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .104


Store and Secure Ribbon Cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .104
Front Access Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .105
Install Lead Wires and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .105
Connect Mains Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .105
Turn Therapy System On . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .106
TROUBLESHOOTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 107112
ERROR CODES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .107-112
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .107
MAINTENANCE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .113
CARING FOR THE THERAPY SYSTEM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 113
Cleaning the Therapy System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .113
Cleaning the Lens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .113
CALIBRATION REQUIREMENTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 113
Calibrating Ultrasound Applicators. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .113
FACTORY SERVICE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .113
WARRANTY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 114

FOREWORD

Intelect Advanced Therapy System

This manual has been written for the users of the Intelect Advanced Therapy Systems. It contains general information on the operation,
precautionary practices, and maintenance information. In order to maximize use, efficiency, and the life of the system, please read this
manual thoroughly and become familiar with the controls, as well as the accessories before operating the system.
This manual contains general safety, operating, maintenance, and care instructions as well as installation instructions for the optional
Channel 3/4 Electrotherapy Module for the users of the Intelect Advanced Therapy two channel electrotherapy and combination systems.
Instructions for additional options such as sEMG, sEMG + Stim, Laser, Battery, and Vacuum are found in their respective User Manuals which
contain operation and installation instructions.
Specifications put forth in this manual were in effect at the time of publication. However, owing to Chattanooga Group's policy of
continual improvement, changes to these specifications may be made at any time without obligation on the part of Chattanooga Group.
Before administering any treatment to a patient, the users of this equipment should read, understand and, follow the information
contained in this manual for each mode of treatment available, as well as the indications, contraindications, warnings, and precautions.
Consult other resources for additional information regarding the application of electrotherapy and ultrasound.
PRODUCT DESCRIPTION
The Intelect Advanced Therapy Systems are two channel electrotherapy and combination systems with the option of adding additional
channels of electrotherapy by installation of the optional Channel 3/4 Electrotherapy Module. Other optional modality modules are
available for separate purchase and may be installed by the end user.
Stay current with the latest clinical developments in the field of electrotherapy, ultrasound, laser therapy, sEMG, and sEMG + Stim. Observe
all applicable precautionary measures for treatment.
Keep informed of appropriate indications and contraindications for the use of electrotherapy, ultrasound, laser therapy, sEMG, and
sEMG+Stim.
This equipment is to be used only under the prescription and supervision of a licensed practitioner.

2005 Encore Medical Corporation or its affiliates, Austin, Texas, USA. Any use of editorial, pictorial, or layout composition of this publication without express written consent from Chattanooga Group
of Encore Medical, L.P. is strictly prohibited. This publication was written, illustrated, and prepared for distribution by Chattanooga Group of Encore Medical, L.P.

SAFETY PRECAUTIONS

Intelect Advanced Therapy System

PRECAUTIONARY DEFINITIONS
The precautionary instructions found in this section and throughout this manual are indicated by specific symbols. Understand these
symbols and their definitions before operating this equipment. The definition of these symbols are as follows;

CautionText with a CAUTION indicator will explain possible safety


infractions that could have the potential to cause minor to
moderate injury or damage to equipment.

DangerText with a DANGER indicator will explain possible safety


infractions that are imminently hazardous situations that would
result in death or serious injury.
Dangerous VoltageText with a Dangerous Voltage indicator serves to inform
the user of possible hazards resulting in the electrical charge
delivered to the patient in certain treatment configurations
of TENS waveforms.

WarningText with a WARNING indicator will explain possible safety


infractions that will potentially cause serious injury and equipment
damage.

NOTE:
Throughout this manual, NOTE may be found. These Notes are
helpful information to aid in the particular area or function being
described.

SAFETY PRECAUTIONS

Intelect Advanced Therapy System

CAUTIONS

Inspect Applicator cables and associated connectors before

Read, understand, and practice the precautionary and operating


instructions. Know the limitations and hazards associated with
using any electrical stimulation or ultrasound device. Observe the
precautionary and operational decals placed on the unit.
DO NOT operate the Intelect Advanced Therapy System when
connected to any unit other than Chattanooga Group devices.
DO NOT operate this unit in an environment where other devices
are being used that intentionally radiate electromagnetic energy in
an unshielded manner.
Ultrasound should be routinely checked before each use to
determine that all controls function normally, especially that
the intensity control does properly adjust the intensity of the
ultrasonic power output in a stable manner. Also, determine that
the treatment time control does actually terminate ultrasonic power
output when the timer reaches zero.
DO NOT use sharp objects such as a pencil point or ballpoint pen to
operate the buttons on the control panel.
This unit should be operated, transported and stored in
temperatures between 15 C and 40 C (59 F and 104 F), with
Relative Humidity ranging from 30%-60%.
Handle Ultrasound Applicator with care. Inappropriate handling of
the Ultrasound Applicator may adversely affect its characteristics.
Before each use, inspect Ultrasound Applicator for cracks, which
may allow the ingress of conductive fluid.

each use.

The Intelect Advanced Therapy System is not designed to prevent


the ingress of water or liquids. Ingress of water or liquids could cause
malfunction of internal components of the system and therefore
create a risk of injury to the patient.
This equipment generates, uses and can radiate radio frequency
energy and, if not installed and used in accordance with the
instructions, may cause harmful interference to other devices in
the vicinity. However, there is no guarantee that interference will
not occur in a particular installation. Harmful interference to other
devices can be determined by turning this equipment on and off.
Try to correct the interference using one or more of the following:
Reorient or relocate the receiving device, increase the separation
between the equipment, connect the equipment to an outlet on a
different circuit from that to which the other device(s) are connected
and consult the factory field service technician for help.
The Nylatex Wraps shipped with this unit contain dry natural rubber
and may cause allergic reactions in patients with allergies to latex.

SAFETY PRECAUTIONS

Intelect Advanced Therapy System

WARNINGS

Powered muscle stimulators should be used only with the leads and

These devices are restricted to sale by, or on the order of, a physician
or licensed practitioner. This device should be used only under the
continued supervision of a physician or licensed practitioner.
For continued protection against fire hazard, replace fuses only with
ones of the same type and rating.
Make certain the unit is electrically grounded by connecting only to a
grounded electrical service receptacle conforming to the applicable
national and local electrical codes.
Care must be taken when operating this equipment around other
equipment. Potential electromagnetic or other interference could
occur to this or to the other equipment. Try to minimize this
interference by not using other equipment in conjunction with it.
The safety of TENS waveforms for use during pregnancy or birth has
not been established.
TENS is not effective for pain of central origin. (This includes
headache.)
TENS should be used only under the continued supervision of a
physician or licensed practitioner.
TENS waveforms have no curative value.
TENS is a symptomatic treatment, and as such, suppresses the
sensation of pain which would otherwise serve as a protective
mechanism.
The user must keep the device out of the reach of children.
Electronic monitoring equipment (such as ECG monitors and ECG
alarms) may not operate properly when TENS stimulation is in use.

electrodes recommended for use by the manufacturer.

In the event that an Error message or Warning appears beginning


with a 2 or 3, immediately stop all use of the system and contact
the dealer or Chattanooga Group for service. Errors and Warnings in
these categories indicate an internal problem with the system that
must be tested by Chattanooga Group or a Field Service Technician
certified by Chattanooga Group before any further operation or use
of the system. Use of a system that indicates an Error or Warning in
these categories may pose a risk of injury to the patient, user or cause
extensive internal damage to the system.
Use of controls or adjustments or performance of procedures other
than those specified herein may result in hazardous exposure to
ultrasonic energy.
Before administering any treatment to a patient you should become
acquainted with the operating procedures for each mode of
treatment available, as well as the indications, contraindications,
warnings, and precautions. Consult other resources for additional
information regarding the application of Electrotherapy and
Ultrasound.
To prevent electrical shock, disconnect the unit from the power
source before attempting any maintenance procedures.
Keep electrodes separated during treatment. Electrodes in contact
with each other could result in improper stimulation or skin burns.
Long term effects of chronic electrical stimulation are unknown.

SAFETY PRECAUTIONS

Intelect Advanced Therapy System

WARNINGS (continued)

Stimulation should not be applied over the anterior neck or mouth.


Severe spasm of the laryngeal and pharyngeal muscles may occur and
the contractions may be strong enough to close the airway or cause
difficulty in breathing.
Stimulation should not be applied transthoracically in that the
introduction of electrical current into the heart may cause cardiac
arrhythmia.
Stimulation should not be applied over swollen, infected, and
inflamed areas or skin eruptions, e.g., phlebitis, thrombophlebitis,
varicose veins, etc.
Stimulation should not be applied over, or in proximity to, cancerous
lesions.
Output current density is related to electrode size. Improper application
may result in patient injury. If any question arises as to
the proper electrode size, consult a licensed practitioner prior to therapy
session.

SAFETY PRECAUTIONS

Intelect Advanced Therapy System

DANGERS

Stimulus delivered by the TENS waveforms of this


device, in certain configurations, will deliver a charge of 25
microcoulombs (C) or greater per pulse and may be sufficient
to cause electrocution. Electrical current of this magnitude
must not flow through the thorax because it may cause a
cardiac arrhythmia.
Patients with an implanted neurostimulation device
must not be treated with or be in close proximity to
any shortwave diathermy, microwave diathermy, therapeutic
ultrasound diathermy, or laser diathermy anywhere on
their body. Energy from diathermy (shortwave, microwave,
ultrasound, and laser) can be transferred through the
implanted neurostimulation system, can cause tissue damage,
and can result in
severe injury or death. Injury, damage, or death can
occur during diathermy therapy even if the implanted
neurostimulation system is turned off.

SAFETY PRECAUTIONS

Intelect Advanced Therapy System

ELECTROTHERAPY INDICATIONS, CONTRAINDICATIONS, AND ADVERSE EFFECTS


INDICATIONS FOR VMS, VMS BURST, RUSSIAN, TENS, HIGH
Contraindications
VOLTAGE PULSED CURRENT HVPC, INTERFERENTIAL AND
This device should not be used for symptomatic local pain relief
PREMODULATED WAVEFORMS
unless etiology is established or unless a pain syndrome has
Relaxation of muscle spasms
been diagnosed.
Prevention or retardation of disuse atrophy
This device should not be used when cancerous lesions are
present in the treatment area.
Increase local blood circulation
Stimulation should not be applied over swollen,
Muscle re-education
infected, inflamed areas, or skin erruptions, e.g. phlebitis,
Maintaining or increasing range of motion
thrombophlebitis, varicose veins, etc.
Additional Indications for Microcurrent, Interferential,
Other contraindications are patients suspected of carrying
Premodulated, VMS, VMS Burst and TENS waveforms
serious infectious disease and or disease, where it is advisable,
Symptomatic relief and management of chronic,
for general medical purposes, to suppress heat or fevers.
intractable pain
Electrode placements must be avoided that apply current
Post-traumatic acute pain
to the carotid sinus region (anterior neck) or transcerebrally
Post-surgical acute pain
(through the head).
Indications for Galvanic Continuous Mode
Safety has not been established for the use of therapeutic
electrical stimulation during pregnancy.
Relaxation of muscle spasm
Powered muscle stimulators should not be used on patients
with cardiac demand pacemakers.
There should not be any use of TENS waveforms on patients with
cardiac demand pacemakers.

SAFETY PRECAUTIONS

Intelect Advanced Therapy System

ELECTROTHERAPY INDICATIONS, CONTRAINDICATIONS, AND ADVERSE EFFECTS (continued)

With TENS waveforms, isolated cases of skin irritation may

ADDITIONAL PRECAUTIONS
Caution should be used for patients with suspected or
diagnosed heart problems.
Caution should be used for patients with suspected or
diagnosed epilepsy.
Caution should be used in the presence of the following:
When there is a tendency to hemorrhage following acute
trauma or fracture.
Following recent surgical procedures when muscle
contraction may disrupt the healing process.
Over a menstruating or pregnant uterus; Over areas of the
skin which lack normal sensation.
Some patients may experience skin irritation or hypersensitivity
due to the electrical stimulation or electrical conductive
medium. The irritation can usually be reduced by using an
alternative conductive medium or an alternative electrode
placement.
Electrode placement and stimulation settings should be based
on the guidance of the prescribing practitioner.
Powered muscle stimulators should be used only with the
lead wires and electrodes recommended for use by the
manufacturer.

occur at the site of electrode placement following long-term


application.
The effectiveness of TENS waveforms is highly dependent upon
patient selection by a person qualified in pain management.
Adverse Effects
Skin irritation and burns beneath the electrodes have been
reported with the use of powered muscle stimulators.
Potential adverse effects with TENS are skin irritation and electrode
burns.

SAFETY PRECAUTIONS

Intelect Advanced Therapy System

ULTRASOUND INDICATIONS AND CONTRAINDICATIONS


INDICATIONS FOR ULTRASOUND
Application of therapeutic deep heat for the treatment of
selected sub-chronic and chronic medical conditions such as:
Relief of pain, muscle spasms, and joint contractures
Relief of pain, muscle spasms, and joint contractures that may
be associated with:
Adhesive capsulitis
Bursitis with slight calcification
Myositis
Soft tissue injuries
Shortened tendons due to past injuries and scar tissues
Relief of sub-chronic, chronic pain, and joint contractures
resulting from:
Capsular tightness
Capsular scarring
Contraindications
This device should not be used for symptomatic local pain relief
unless etiology is established or unless a pain syndrome has
been diagnosed.
This device should not be used when cancerous lesions are
present in the treatment area.
Stimulation should not be applied over swollen,
infected, inflamed areas, or skin erruptions, e.g. phlebitis,
thrombophlebitis, varicose veins, etc.

Other contraindications are patients suspected of carrying


serious infectious disease and disease where it is advisable for
general medical purposes to suppress heat or fevers.
This device should not be used over or near bone growth
centers until bone growth is complete.
This device should not be used over the thoracic area if the
patient is using a cardiac pacemaker.
This device should not be used over a healing fracture.
This device should not be used over or applied to the eye.
This device should not be used over a pregnant uterus.
This device should not be used on ischemic tissues in
individuals with vascular disease where the blood supply would
be unable to follow the increase in metabolic demand and
tissue necrosis might result.
Additional Precautions
Additional precautions should be used when ultrasound is
used on patients with the following conditions:
Over an area of the spinal cord following;
Laminectomy, i.e., when major covering tissues have been
removed.
Over anesthetic areas.
On patients with hemorrhagic diatheses.

NOMENCLATURE

Intelect Advanced Therapy System

INTELECT ADVANCED ELECTROTHERAPY AND COMBINATION THERAPY SYSTEMS


Two (2) Channel Electrotherapy System

Two (2) Channel Combination System


4

1
6

6
2

2
3

3
5

1.
2.
3.
4.
5.
6.

1. Two Channel Combination System


2. User Interface (See Page 12)
3. Front Access Panel
4. Rear Access Panel
5. Patient Data Card and sEMG Data Card access port.
6. Multimedia Card (MMC) access port.
Ultrasound Applicator (5cm2 shown) Combination Systems Only

Two (2) Channel Electrotherapy System


User Interface (See Page 12)
Front Access Panel
Rear Access Panel
Patient Data Card and sEMG Data Card access port.
Multimedia Card (MMC) access port.
10

NOMENCLATURE

Intelect Advanced Therapy System

INTELECT ADVANCED ELECTROTHERAPY AND COMBINATION THERAPY SYSTEMS (continued)


Front Access Panel
Rear Access Panel
1
7
2
5
3
4
1

3
2

5
4

7
6
6

1. Front Access Panel Lanyard


When reinstalling the Front Access Panel, make certain the
Lanyard does not become kinked.
2. Operator Remote Control Connector
3. Patient Interrupt Switch Connector
4. Channel 1 Lead Wire Connector
5. Channel 2 Lead Wire Connector
6. Microcurrent Probe Connector
7. Ultrasound Applicator Connector

1.
2.
3.
4.
5.
6.
7.
11

Screen Contrast Control (Not functional on Color Systems)


Power On/Off Switch
Technical Maintenance Port
Fuses
Mains Power Cord
Rear Access Panel
Serial Decal

NOMENCLATURE

Intelect Advanced Therapy System

USER INTERFACE
1
15

2
3

16

14
4
13
12
5

11
10
9

8
7
6
12

1. Rear Access Panel (See Page 11)


2. User Interface (Color Shown)
3. Ultrasound LED Coupling Indicator
(Combination only)
4. Ultrasound Applicator- 5 cm2 Standard.
(Optional 1 cm2, 2 cm2 and 10 cm2 )
applicators available (Combination only)
5. Intensity Knob
6. Cable and Lead Wire Hook
7. Front Access Panel (See Page 11)
8. Start Button
9. Pause Button
10. Stop Button
11. Clinical Resources Library Button
12. Home Screen button
13. Back Button
14. Patient Data Card and sEMG Data Card Port
15. User Set Up and Parameter Control buttons
16. Multimedia Card (MMC) Port

NOMENCLATURE

Intelect Advanced Therapy System

SYMBOL DEFINITIONS
Below are the definitions for all of the symbols used in the Intelect Advanced hardware and software. Study and learn these symbols before
any operation of the system.
System
Software Symbols

System Hardware Symbols


CONTRAST CONTROL
NOT FUNCTIONAL ON
COLOR SYSTEMS
ON/OFF SWITCH

PATIENT INTERRUPT
SWITCH
THERAPY
INTENSITY
CONTROL

MOVE UP

START TREATMENT

DECREASE
INTENSITY

CHANNEL 2
LEAD WIRES

PAUSE
TREATMENT

MOVE LEFT
CLINICAL
RESOURCES
LIBRARY

ACCEPT AND
RETURN

MICROCURRENT PROBE

PAUSE TREATMENT

BACK

CHANNEL 1/2
OPERATOR
REMOTE
CONTROL
OPTIONAL

DO NOT ACCEPT
AND RETURN

ULTRASOUND
APPLICATOR

Channel 3/4
Electrothrapy
Module

MOVE DOWN

CHANNEL 1
LEAD WIRES

MOVE RIGHT
HOME

STOP TREATMENT

Operator Remote
INCREASE
INTENSITY

DATA PORT

MULTIMEDIA CARD,
PATIENT DATA CARD,
AND SEMG DATA CARD

Optional Module and Accessory Symbols

PAD CONTACT QUALITY


SINGLE CHANNEL GRAPH

MANUAL
STIMULATION

Battery Module

13

CHANNEL 3 LEAD WIRES

CHANNEL 4 LEAD WIRES

MICROCURRENT PROBE

CHARGE LEVEL
BATTERY CHARGING

PAD CONTACT QUALITY


DUAL CHANNEL GRAPH

PATIENT INTERRUPT SWITCH

CHANNEL 3/4 OPERATOR


REMOTE CONTROL
OPTIONAL

NOMENCLATURE

Intelect Advanced Therapy System

Below are the definitions for all of the unique terminology used throughout this manual. Study these and become familiar with these
terms for ease of system operation and familiarization with the components and control functionality of the Intelect Adavnced Therapy
System. Some of these terms and definitions refer to a specific button or control on the system. Refer to page 13 for Symbol Definitions.
GENERAL TERMINOLOGY
Back button
The dedicated button on the Main unit, below the display, that
each time pressed takes the user back one screen at a time.

ULTRASOUND
3

Previous Page button


The button used in some modalities and functions that will take
the user back one page when reading multiple pages of text.
UP and DOWN Arrows
Controls used in various modality parameter screens to navigate or
change a value up or down within the parameter.

Electrotherapy
Refers to the Electrical muscle or nerve Stimulation modalities of
the system.

1. Sound Head
That component of the Applicator that makes contact with the
patient during Ultrasound or Combination therapy.
2. Applicator
The assembly that connects to the System and incorporates the
Sound Head.

System
The primary system with all controls and functions.
Module
Any optional modular modality component designed for
installation onto the System.

3. Coupling LED
The component of the Applicator which indicates if the
Sound Head is Coupled or Uncoupled on the the treatment
area.
14

SPECIFICATIONS

Intelect Advanced Therapy System

SYSTEM SPECIFICATIONS

DIMENSIONS
Width
Combination System . . . . . . . . . . . . . . . . . . . . . . . . . . 28.9 cm (11.375)
Electrotherapy System . . . . . . . . . . . . . . . . . . . . . . . . . . . 24.8 cm (9.750)
Depth (Combination and Electrotherapy System) 32.4 cm (12.750)
Height (Combination and Electrotherapy System) . 22.2 cm (8.750)
Standard Weight
Two Channel Combination System . . . . . . . . . . . . . . . . . 3.2 kg (7 lbs)
Two Channel Electrotherapy System . . . . . . . . . . . . . . . . 2.7 kg (6 lbs)
Power (Combination and Electrotherapy Units)
Input . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 100 - 240 V - 1.0 A, 50/60 Hz
Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . +12 V, 8.3 A
Fuses . . . . . . . . . . . . . . . . . . . . . Two 6.3A Time Lag (Part Number 71772)
Electrical Class . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .CLASS I
Electrical Type
Ultrasound . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . TYPE B
Electrotherapy and sEMG . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . TYPE BF
Regulatory Compliance
UL/IEC/EN 60601-1
IEC/EN 60601-1-2
IEC 60601-2-5
IEC 60601-2-10

HEIGHT

DEPTH
WIDTH

NOTE:
All waveforms except High Voltage Pulsed Current (HVPC) have been
designed with a 200mA current limit.
VMS, VMS Burst and all TENS waveform output intensities are
measured, specified and listed to peak, not peak to peak.

0413

15

SPECIFICATIONS

Intelect Advanced Therapy System

WAVEFORM SPECIFICATIONS
IFC (Interferential) Traditional (4 Pole)

TENS- Asymmetrical Biphasic

Interferential Current is a medium frequency waveform. Current


is distributed through of two channels (four electrodes). The
currents cross each other in the body at the area requiring
treatment. The two currents interfere with each other at this
crossing point, resulting in a modulation of the intensity (the
current intensity increases and decreases at a regular frequency).
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Carrier Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2000-10,000 Hz
Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-200 Hz
Sweep Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 sec
Sweep Low Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 Hz
Sweep High Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 Hz
Scan Percentage . . . . . . . . . . . . . . . . . . . . . . . . . . Static, 10%, 40%, 100%
Amplitude . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 mA RMS into 500 ohm
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Minutes
Available on Channel . . . . . . . . . . . . . . . . . . . . . . . . . . . .1&2, 3&4 Option

The Asymmetrical Biphasic waveform has a short pulse duration.


It is capable of strong stimulation of the nerve fibers in the skin
as well as of muscle tissue. This waveform is often used in TENS
devices. Because of its short pulse, the patient typically tolerates
the current well, even at relatively high intensities.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-110 mA
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . Adjustable 20-1,000 sec
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-250 Hz
Mode Selection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Burst Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-10 bps
Frequency Modulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-250 Hz
Amplitude Modulation . . . . . . . . . . . . Off, 40%, 60%, 80% and 100%
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Stimulus delivered by the TENS waveforms of this device, in


certain configurations, will deliver a charge of 25 microcoulombs
(C) or greater per pulse and may be sufficient to cause
electrocution. Electrical current of this magnitude must not flow
through the thorax because it may cause a cardiac arrhythmia.

*CC= Constant Current


CV= Constant Voltage
16

SPECIFICATIONS

Intelect Advanced Therapy System

WAVEFORM SPECIFICATIONS (continued)


TENS- Symmetrical Biphasic

TENS- Alternating Rectangular

The Symmetrical Biphasic waveform has a short pulse duration


and is capable of strong stimulation of nerve fibers in the skin
and in muscle. This waveform is often used in portable muscle
stimulation units, and some TENS devices. Because of its short
pulse duration, the patient typically tolerates the current well,
even at relatively high intensities.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . Adjustable 20-1,000 sec
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-250 Hz
Mode Selection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Burst Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-4 bps
Frequency Modulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-250 Hz
Amplitude Modulation . . . . . . . . . . . . Off, 40%, 60%, 80% and 100%
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

The Alternating Rectangular waveform is an interrupted biphasic


current with a rectangular pulse shape. This waveform is
commonly used as a pain management application.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 mA
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . Adjustable 20-1,000 sec
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 Hz
Mode Selection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Burst Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-10 bps
Frequency Modulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-250 Hz
Amplitude Modulation . . . . . . . . . . . . Off, 40%, 60%, 80% and 100%
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Stimulus delivered by the TENS waveforms of this device, in


certain configurations, will deliver a charge of 25 microcoulombs
(C) or greater per pulse and may be sufficient to cause
electrocution. Electrical current of this magnitude must not flow
through the thorax because it may cause a cardiac arrhythmia.

*CC= Constant Current


CV= Constant Voltage
17

SPECIFICATIONS

Intelect Advanced Therapy System

WAVEFORM SPECIFICATIONS (continued)


TENS- Monophasic Rectangular

High Voltage Pulsed Current (HVPC)

The Monophasic Rectangular waveform is an interrupted


unidirectional current with a rectangular pulse shape. This
waveform is commonly used with electrodiagnostic testing and
clinically to stimulate denervated muscle.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-110 mA
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . Adjustable 20-1,000 sec
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 Hz
Mode Selection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Burst Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-10 bps
Frequency Modulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-250 Hz
Amplitude Modulation . . . . . . . . . . . . . Off, 40%, 60%, 80%and 100%
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

The High Voltage Pulsed Current (HVPC) has a very brief pulse
duration characterized by two distinct peaks delivered at
high voltage. The waveform is monophasic (current flows in
one direction only). The high voltage causes a decreased skin
resistance making the current comfortable and easy to tolerate.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Electrodes or Probe
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-500 V
Polarity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Positive or Negative
Ramp. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.5 sec, 1 sec, 2 sec, 5 sec
Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Peak Current or Volts
Sweep . . . . . . . . . . . . . .Continuous, 80/120 pps, 1/120 pps, 1/10 pps
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-120 pps
Cycle Time. . . . . .5/5, 4/12, 10/10, 10/20, 10/30, 10/50, Continuous
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Min
Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

Stimulus delivered by the TENS waveforms of this device,


in certain configurations, will deliver a charge of 25
microcoulombs (C) or greater per pulse and may be
sufficient to cause electrocution. Electrical current of this
magnitude must not flow through the thorax because it may
cause a cardiac arrhythmia.

*CC= Constant Current


CV= Constant Voltage
18

SPECIFICATIONS

Intelect Advanced Therapy System

WAVEFORM SPECIFICATIONS (continued)


Diadynamic Waveforms
The Diadynamic waveforms are rectified alternating currents. The
alternating current is modified (rectified) to allow the current to
flow in one direction only.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
Available on channels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1, 2, 3, 4
MF: (Monophas Fixe) - Frequency of 50 Hz: phase duration of
10 ms followed by a pause of 10 ms.
DF: (Diphas Fixe) - Frequency of 100 Hz: phase duration of 10 ms
followed immediately by another identical phase of 10 ms.
CP: (Modul en Courtes Priodes) - 1 second of MF followed
abruptly by 1 second of DF.
LP: (Modul en Longues Priodes) - Rhythmical fluctuation
between 2 MF currents.
CP-iso: (Courtes Periodes Isodynamic) - A combination of MF and
DF waveforms.
CP-id: Same as CP-iso.
MF+CP: A period of MF followed by a period of CP.
MF+CP-id: A period of MF followed by a period of CP-ID.
DF+LP: A period of DF followed by a period of LP.
DF+CP: A period of DF followed by a period of CP.

VMSTM
VMS is a symmetrical biphasic waveform with a 100 sec interphase
interval. Because the pulse is relatively short, the waveform has a low
skin load, making it suitable for applications requiring high intensities,
such as in muscle strengthening protocols.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-255 mA
Channel Mode . . . . . . . . . . . . . . . . . . . . . . . . . Single, Reciprocal, Co-Contract
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20-1000sec
Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Anti-Fatigue . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Off or On
Set Intensity . . . . . . . . . . . . . . . . . . . . . Individual Channel Intensity Setting in
Reciprocal and Co-Contract modes
Cycle Time . . . . . . . . . . .Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 pps
Ramp . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0.5 sec, 1 sec, 2 sec, 5 sec
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

*CC= Constant Current


CV= Constant Voltage
19

SPECIFICATIONS

Intelect Advanced Therapy System

WAVEFORM SPECIFICATIONS (continued)


Russian

IFC Premodulated (2p)

Russian Current is a sinusoidal waveform, delivered in bursts or


series of pulses. This method was claimed by its author (Kots)
to produce maximal muscle strengthening effects without
significant discomfort to the patient.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Pads
Output Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 mA
Channel Mode . . . . . . . . . . . . . . . . . . . . . . . . . Single, Reciprocal, Co-Contract
Duty Cycle. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10%, 20%, 30%, 40%, 50%
Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Anti-Fatigue . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Off or On
Cycle Time. . . . . .5/5, 4/12, 10/10, 10/20, 10/30, 10/50, Continuous
Burst Frequency (Anti-Fatigue Off ) . . . . . . . . . . . . . . . . . . . . 20-100 pps
Ramp. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.5, 1, 2 and 5 sec
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

Premodulated Current is a medium frequency waveform. Current


comes out of one channel (two electrodes). The current intensity
is modulated: it increases and decreases at a regular frequency
(the Amplitude Modulation Frequency).
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Pads
Output Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 mA
Carrier Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2000-10,000 Hz
Beat Fixed (Sweep Off ) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 Hz
Sweep Low Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-149 Hz
Sweep High Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . 81-200 Hz
Cycle Time . . . . . . . . . . .Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50
Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Carrier Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2,000-10,000 Hz
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Min
Available on Channel . . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

*CC= Constant Current


CV= Constant Voltage
20

SPECIFICATIONS

Intelect Advanced Therapy System

WAVEFORM SPECIFICATIONS (continued)


Microcurrent

VMSTM Burst

Microcurrent is a monophasic waveform of very low intensity.


The literature reports beneficial effects of this waveform in the
treatment of wounds. The physiological working mechanism of
this effect is as yet not clearly understood. It is thought to
stimulate tissue healing by stimulating the 'current of injury', a
current which naturally occurs in healing tissue.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Electrodes or Probe
Output Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-1000.0 A
Polarity . . . . . . . . . . . . . . . . . . . . . . . . . .Positive, Negative or Alternating
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Min
Available on channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

VMS Burst is a symmetrical biphasic waveform delivered in a burst


format. Because the pulse is relatively short, the waveform has a
low skin load, making it suitable for applications requiring high
intensities, such as in muscle strengthening protocols.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-255 mA
Channel Mode . . . . . . . . . . . . . . . . . . . . . . . . . Single, Reciprocal, Co-Contract
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20-1000 sec
Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Anti-Fatigue . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Off or On
Set Intensity . . . . . . . . . . . . . . . . . . . . . .Individual Channel Intensity Setting in
Reciprocal and Co-Contract modes
Cycle Time . . . . . . . . . . .Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 pps
Ramp . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0.5 sec, 1 sec, 2 sec, 5 sec
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

*CC= Constant Current


CV= Constant Voltage
21

SPECIFICATIONS

Intelect Advanced Therapy System

WAVEFORM SPECIFICATIONS (continued)


MONOPHASIC: Monophasic Rectangular Pulsed

MONOPHASIC: Monophasic Triangular Pulsed


The Monophasic Triangular Pulsed waveform is an interrupted
unidirectional current with a triangular pulse shape.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-80 mA
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.1-500.0 ms
Phase Interval . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5000 ms
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

The Monophasic Rectangular Pulsed waveform is an interrupted


unidirectional current with a rectangular pulse shape.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.1-500.0 ms
Phase Interval . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5000 ms
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

Stimulus delivered by the TENS waveforms of this device, in certain


configurations, will deliver a charge of 25 microcoulombs (C) or
greater per pulse and may be sufficient to cause electrocution.
Electrical current of this magnitude must not flow through the
thorax because it may cause a cardiac arrhythmia.

22

SPECIFICATIONS

Intelect Advanced Therapy System

WAVEFORM SPECIFICATIONS (continued)


GALVANIC: Continuous

GALVANIC: Interrupted
Galvanic Current is a direct current flowing in one direction only.
The current can be continuous or interrupted.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA
Polarity Reversal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . On or Off
With Polarity Reversal On, Polarity will change every five minutes.
Cycle Time . . . . . . . . . . .Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

Galvanic Current is a direct current flowing in one direction only.


The current can be continuous or interrupted.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA
Polarity Reversal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . On or Off
With Polarity Reversal On, Polarity will change every five minutes.
Cycle Time . . . . . . . . . . .Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

23

SPECIFICATIONS

Intelect Advanced Therapy System

WAVEFORM SPECIFICATIONS (continued)


SURGED: Monophasic Rectangular

Trbert (Ultrareiz)

A series of rectangular, monophasic pulses. The pulses surge to


maximum power, hold and then decrease before the pause. This
waveform is well suited for muscle strengthening.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.2-5.0 ms
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-60 Hz
Surges . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1/min - 20/min
Pause . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-57 sec
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

It is a monophasic waveform with a phase duration of 2 ms and a


pause of 5 ms resulting in a frequency of approximately 143 Hz.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA
Polarity Reversal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . On or Off
With Polarity Reversal On, Polarity will change every 7.5 minutes.
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

Stimulus delivered by the TENS waveforms of this device, in


certain configurations, will deliver a charge of 25 microcoulombs
(C) or greater per pulse and may be sufficient to cause
electrocution. Electrical current of this magnitude must not flow
through the thorax because it may cause a cardiac arrhythmia.

24

SPECIFICATIONS

Intelect Advanced Therapy System

WAVEFORM SPECIFICATIONS (continued)


SURGED: Monophasic Triangular
A series of triangular, monophasic pulses. The pulses surge to
maximum power, hold and then decrease before the pause. This
waveform is well suited for muscle strengthening.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.2-5.0 ms
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-60 Hz
Surges . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1/min - 20/min
Pause . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-57 sec
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

Stimulus delivered by the TENS waveforms of this device, in


certain configurations, will deliver a charge of 25 microcoulombs
(C) or greater per pulse and may be sufficient to cause
electrocution. Electrical current of this magnitude must not flow
through the thorax because it may cause a cardiac arrhythmia.

25

SPECIFICATIONS

Intelect Advanced Therapy System

ULTRASOUND SPECIFICATIONS
Ultrasound
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 MHz, 5%; 3.3 Mhz, 5%
Duty Cycles. . . . . . . . . . . . . . . . . . . . . . . . . . . 10%, 20%, 50%, Continuous
Pulse Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 100Hz
Pulse Duration . . . . . . . 1 mSec, 20%; 2 mSec, 20%; 5 mSec, 20%
Output Power
10 cm2 Crystal . . . . . . . . . . . . . . . . .0-20 W at 1MHz, 0-10 W at 3.3 MHz
5 cm2 Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-10 W, 1 and 3.3 MHz
2 cm2 Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-4 W, 1 and 3.3 MHz
1 cm2 Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-2 W 3.3 MHz Only
Amplitude . . . . . . . . . . . . . . . . . . . .0 to 2.5 w/cm2 in continuous mode,
0-3 w/cm2 in pulsed modes
Output accuracy. . . . . . . . . . . . . . . . . . . 20% above 10% of maximum
Temporal Peak to Average Ratio: . . . . 2:1, 20%, at 50% Duty Cycle
5:1, 20%, at 20% Duty Cycle
9:1, 20%, at 10% Duty Cycle
Beam Nonuniformity Ratio . . . . . . . . . . . . . . . . . . . . . . 5.0 : 1 maximum
Beam Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Collimating

Effective Radiating Areas. . . . . . . . . . . . 10 cm2 Crystal: 8.5 cm2, 1.5


5 cm2 Crystal: 4.0 cm2, 1.0
2
2 cm Crystal: 1.8 cm2, +0.2/- 0.4
1 cm2 Crystal: 0.8 cm2, +0.2/-0.4
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-30 min
Head Warming Feature
The Head Warming feature of an Intelect Advanced Combination
Therapy System utilizes Ultrasound output resulting in warming
of the Sound Head to increase patient comfort.
With Head Warming enabled, ultrasound is emitted without
pressing the Start button. The Applicator LED will not illuminate
during the Head Warming period. US Channel will indicate "Head
Warming".
Output . . . . . . . . . . . . . . . . . . . . . . . 0 - 50% Cycling of maximum power
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.3 Mhz
Sound Head Temperature . . . . . . . . . 29.4 C - 43.3 C (85 F - 110 F)

Do not apply the Ultrasound Applicator to the patient during the Head
Warming period. Applicator must remain in Applicator Hook duing the
Head Warming period.

26

SET UP

Intelect Advanced Therapy System

INTELECT ADVANCED COLOR SERIES THERAPY SYSTEMS


Remove the Therapy System and all accessories from shipping cartons. Visually inspect for damage. Report any damage to the carrier.
Color Series
Color Series Standard Features
Mains Power Cords
Optional Accessories
Order No.

Description
(or)

Qty

2765CS

Two Channel Electrotherapy System

2762CC

Two Channel Combination System

27378

Electrotherapy Accessory Kit- Includes the following:

27312

Channel 1 Lead Wire

27313

Channel 2 Lead Wire

10648

Nylatex Wrap

79967

6 x 8 cm Carbon Electrodes

79970

6 x 8 cm Electrode Sponges

42044

7 cm (2.75") Round Disposable Electrodes (4 per pack)

27469

Patient Interrupt Switch for Channels 1/2

27335

5 cm2 Ultrasound Applicator (Combination Systems Only)

4248

Conductor TM Transmission Gel- 9 oz Bottle (Combination Systems Only)

27085

Anatomical/Pathological Library (MMC Card)

27465

Patient Data Card

2771

sEMG Module (Factory Installed)

27567

sEMG Accessory Kit- Includes the Following

27321

sEMG Channel 1 (A) Lead Wire

27322

sEMG Channel 2 (B) Lead Wire

77725

Intravaginal Probe

42061

3.2 cm (1.25") Round Disposable Electrode Pack (4 per pack)

27455

User Manual (CD-ROM)

Order No.

Description

Order No.

2770
2767
2766
2771
27567
2785
2774
2775
2768

21284
78121
20971
20972
20973
20974
20975
20976
20977

27779
27176
27300
27167
27516
27780
27508
27079
27333

Two Channel Electrotherapy Module


NiMH Battery Module
Laser Therapy Module
sEMG Module
sEMG Accessory Kit
Vacuum Electrode Module
Vacuum Electrode Module w/Cart
Therapy System Cart
Patient Data Management System- Includes
the following:
Version 1.0 PC Software (Windows)
Card Reader
USB Cable
sEMG Data Card
sEMG Data Card Sleeve
User Manual (on Software CD)
Operator Remote (Ch 1/2)
Operator Remote (Ch 3/4)
1 cm2 US Applicator (Combination Only)

27334
27336

2 cm2 US Applicator (Combination Only)


10 cm2 US Applicator (Combination Only)

27

Type
Euro
US
Australian
Swiss
UK
Danish
Japanese
Indian
Israeli

Qty
1
1
1
1
1
1
1
1
1

NOTE:
The Power Cord shipped with
the System will accommodate
the electrical requirements for
the country of use.

SET UP

Intelect Advanced Therapy System

INTELECT ADVANCED MONOCHROMATIC SERIES THERAPY SYSTEMS


Remove the Therapy System and all accessories from shipping cartons. Visually inspect for damage. Report any damage to the carrier.
Monochromatic Series
Optional Accessories

Monochromatic Series Standard Features


Order No.

Description
(or)

Mains Power Cords

Qty

Order No.

Description

Order No.

2770
2767
2766
2771
27567
2785
2774
2775
2768

21284
78121
20971
20972
20973
20974
20975
20976
20977

27779
27176
27300
27167
27516
27780
27508
27079
27333

Two Channel Electrotherapy Module


NiMH Battery Module
Laser Therapy Module
sEMG Module
sEMG Accessory Kit
Vacuum Electrode Module
Vacuum Electrode Module w/Cart
Therapy System Cart
Patient Data Management System- Includes
the following:
Version 1.0 PC Software (Windows)
Card Reader
USB Cable
sEMG Data Card
sEMG Data Card Sleeve
User Manual (on Software CD)
Operator Remote (Ch 1/2)
Operator Remote (Ch 3/4)
1 cm2 US Applicator (Combination Only)

27334
27336

2 cm2 US Applicator (Combination Only)


10 cm2 US Applicator (Combination Only)

2773MS

Two Channel Electrotherapy System

2772MC

Two Channel Combination System

27378

Electrotherapy Accessory Kit- Includes the following:

27312

Channel 1 Lead Wire

27313

Channel 2 Lead Wire

10648

Nylatex Wrap

79967

6 x 8 cm Carbon Electrodes

79970

6 x 8 Electrode Sponges

42044

7 cm (2.75") Round Disposable Electrodes (4 per Pack)

27469

Channel 1/2 Patient Interrupt Switch

27335

5 cm2 Ultrasound Applicator (Combination Systems Only)

4248

ConductorTM Transmission Gel- 9 oz Bottle (Combination Systems Only)

27085

Anatomical/Pathological Library (MMC Card)

27465

Patient Data Card

27455

User Manual (CD-ROM)

28

Type
Euro
US
Australian
Swiss
UK
Danish
Japanese
Indian
Israeli

Qty
1
1
1
1
1
1
1
1
1

NOTE:
The Power Cord shipped with
the System will accommodate
the electrical requirements for
the country of use.

SET UP
THERAPY SYSTEM SET UP
Accessing Operator Utilities
Plug unit into wall outlet.

Intelect Advanced Therapy System

Select the row of alpha or numeric


characters desired by pushing the
button beside the corresponding
row. Select the desired character in
the row by pressing the row button
until the desired letter is framed.

POWER SWITCH

Turn system On.

Press the Home and Back buttons


simultaneously.

Once selection is framed, press the


Accept and Return Arrow button.
The character just chosen will
display in the top of the screen and
the cursor will advance to the next
character.
To go back a character press the
Move Left Arrow button. To delete
the character, press the Delete
button.

To return to the System Home


screen, press the Home button.

Clinic Name
Press Clinic Name button.

CLINIC NAME BUTTON

Once Clinic Name is completed,


press the Save button.
To discard entry, press the Back
button.
29

SELECT ROW AND CHARACTER BUTTONS

MOVE
LEFT

ACCEPT AND
RETURN

DELETE

SAVE

BACK

SET UP

Intelect Advanced Therapy System

THERAPY SYSTEM SET UP (continued)


Restore Default Protocols
Press Restore Default Protocols
RESTORE DEFAULT
button.
PROTOCOLS BUTTON

Press Yes button to restore the


Protocols to Factory Settings. This
will permanently remove all User
Protocols and Sequences.

Restore Default Unit Settings


Press the Restore Default Unit
Settings button to restore the
system defaults. This control will
neither change the Date and
Time nor affect any of the Clinical
Protocols stored in the system.

After the settings have been


restored, a message will appear
stating that the Default Unit
Settings are restored. Press any
button to return to Utilities
screen.

PRESS YES BUTTON TO


RESTOREPROTOCOLS

If it is not desired to permanently


remove all of the User Protocols
and User Sequences from the
System, press the No button.
PRESS NO BUTTON TO
KEEP PROTOCOLS
AS THEY ARE

30

RESTORE DEFAULT UNIT


SETTINGS BUTTON

SET UP

Intelect Advanced Therapy System

THERAPY SYSTEM SET UP (continued)


Erase Patient Data Card
Install Patient Data Card to be
INSERT
erased into Patient Data Card
PATIENT
CARD
Access Port on the system.
Press Erase Patient Card button.

Press the Yes button to erase


all data from Patient Data Card.
Press the No button to keep all
data on Patient Data Card.

YES
BUTTON

Set Date and Time


Press Set Date and Time button.

ERASE PATIENT
CARD BUTTON

SET DATE
AND TIME
BUTTON

NO
BUTTON

Press the UP or Down Arrow


button for the respective area
until desired change is displayed.

PRESS THE RESPECTIVE UP OR DOWN


ARROW BUTTONS TO CHANGE

After all desired changes are


made, press the Back button to
return to the Utilities screen.
After Patient Data Card is
erased, a verification message
will appear. Press any button to
return to the Utilities screen.

YES
BUTTON

YES
BUTTON

NO
BUTTON

BACK
BUTTON

31

SET UP
THERAPY SYSTEM SET UP (continued)
Setting System Volume
Press Volume button until
the desired system volume is
achieved. There are six settings:
Off, X-Low, Low, Med, High, and
X-High.
Each time the Volume button is
pressed the setting displayed will
emit three beep tones at that
level.

Intelect Advanced Therapy System

Ultrasound Coupling
This warning system works in conjunction with the Applicator
LED to alert the user should the Sound Head become uncoupled
from the patient. Press the US Coupling button until the desired
setting is displayed. There are four different alarm settings and an
Off setting.

VOLUME
BUTTON

Pause and Beep


Pauses Treatment Time and
emits an audible beep. When
the Applicator Sound Head is
re-coupled to the patient, the
Treatment Timer will automatically
restart.
Pause and No Beep
Pauses Treatment Timer. When
the Applicator Sound Head is
re-coupled to the patient, the
Treatment Timer will automatically
restart.
Beep
Emits an audible beep.
No Beep
No beep is emitted.
Off
Turns the Ultrasound
Coupling feature.
32

US COUPLING
BUTTON

SET UP
THERAPY SYSTEM SET UP (continued)
Display Unit Version Information
Press the Display Unit Version
Information button to show
the system software versions
installed.

Intelect Advanced Therapy System

Pad Contact Quality


The Pad Contact Quality feature indicates to the user the contact
quality of the electrodes on the patient. This function, if On,
displays a bar graph at the bottom of Treatment Review screen for
the following waveforms only:

PRESS DISPLAY UNIT


VERSION BUTTON TO VIEW
SOFTWARE VERSIONS

IFC Traditional (4p):


Dual Channel Graph
IFC Premod (2p):
Single Channel Graph
Russian:
Single Channel Graph
To turn on, press Pad Contact
Quality button until On is
displayed.
Single Channel Waveforms will
display a single bar graph. Dual
Channel waveforms will display a
double bar graph.
Contact quality is measured by
the amount of the graph filled
with black.
An ideal contact quality is 75% or
more of the graph filled.

Press the Back button to return


the Operator Utilities screen.

BACK
BUTTON

PAD CONTACT QUALITY


BUTTON

SINGLE CHANNEL GRAPH

GOOD CONTACT
QUALITY

DUAL CHANNEL GRAPH


CHANNEL 1:
GOOD CONTACT QUALITY

CHANNEL 2:
NO CONTACT QUALITY

33

SET UP
THERAPY SYSTEM SET UP (continued)
Select Language
To change the language
displayed on the system, press
the Language button until the
desired language is displayed.
Press Home button to set the
language and return to Home
screen.
If Unit Default Settings are
restored, the language will revert
back to English.

Intelect Advanced Therapy System

Connecting Accessories to the Therapy System


Install Lead Wires, Ultrasound Applicator, Patient Interrupt Switch,
and any other accessories according to the Front Access Panel as
illustrated below. Refer to page 13 for Symbol Definitions.

LANGUAGE
BUTTON

MICROCURRENT PROBE
OPTIONAL

OPERATOR REMOTE
OPTIONAL

PRESS HOME BUTTON


TO SET LANGUAGE
CHANNEL 1
CHANNEL 1/2
PATIENT INTERRUPT SWITCH LEAD WIRE
BLACK

34

CHANNEL 2
LEAD WIRE
GREY

ULTRASOUND APPLICATOR
COMBO SYSTEMS ONLY

PATIENT PREPARATION

Intelect Advanced Therapy System

ELECTROTHERAPY PATIENT PREPARATION


Electrode Placement
Examine the skin for any wounds and clean the skin.
Apply the electrodes to the treatment area.
Ensure the electrodes are applied securely to the skin.
Ensure good contact between each electrode and the skin.
Check the electrode contact regularly during the treatment.
Examine the skin again after the treatment.
Choose electrodes that fit the anatomy.
View the Electrode Placement recommendations in the
Treatment Review screen for the particular modality being used
for treatment as a reference point only prior to administering
treatment.
Refer to the respective electrode type instructions on pages 37
through 38.
Follow electrode manufacturer instructions.

Keep electrodes separated during treatment. Electrodes in contact with


each other could result in improper stimulation or skin burns.
Output current density is related to electrode size. Improper
application may result in patient injury. If any question arises as to the
proper electrode size, consult a licensed practitioner prior to therapy
session.
Powered muscle stimulators should be used only with the leads and
electrodes recommended for use by the manufacturer.

35

PATIENT PREPARATION

Intelect Advanced Therapy System

ELECTROTHERAPY PATIENT PREPARATION (continued)


Dura-Stick Electrodes
Chattanooga Group Dura-Stick Electrodes are a self adhesive, single
patient, one time use disposable product designed specifically for
use with Chattanooga Group Electrotherapy systems.
It is recommended that Chattanooga Group Dura-Stick Electrodes
be used whenever possible to ensure the highest level of contact
with the treatment area and most uniform delivery of the
prescribed electrotherapy treatment.
Properly dispose of used Dura-Stick Electrodes upon completion of
the therapy session.

Reusable Carbon Electrodes


If used for delivery of electrotherapy, the Carbon Electrodes must
be inserted into the sponges moistened with distilled water prior to
placement on the patient.
These Carbon Electrodes should be secured to the treatment area
using the Nylatex Wraps shipped with the Therapy System.

36

PATIENT PREPARATION

Intelect Advanced Therapy System

ELECTROTHERAPY PATIENT PREPARATION (continued)


Dura-Stick Electrode Instructions
Connecting Lead Wires
Securing Electrodes
Insert the lead with the Red (+) electrode
Remove the Dura-Stick Electrodes from
connector into one Dura-Stick Electrode.
the protective backing and apply to the
Insert the lead with the Black (-) electrode
treatment area as prescribed. Ensure the
connector into the other electrode.
entire electrode surface is in contact with
Make certain the lead wires are
patient skin by pressing into place.
seated completely into the electrodes.
NOTE:
Use of conductive medium or sponges is
not required or recommended. Dura-Stick
Electrodes are manufactured to ensure
the optimum conductivity during therapy
when properly applied.
LEAD WIRE SEATED
RED +
LEAD WIRE

BLACK
LEAD WIRE

37

PATIENT PREPARATION

Intelect Advanced Therapy System

ELECTROTHERAPY PATIENT PREPARATION (continued)


Reusable Carbon Electrodes
Connecting Lead Wires
Insert the lead with the Red (+) electrode
connector into electrode. Insert the lead
with the black (-) electrode connector into
the other electrode.
Make certain the lead wires are seated
completely into the electrodes.

Conductive Medium
Use wet sponges or liberally apply
Conductor Transmission Gel to electrode
prior to placement on patient.

Securing Electrodes
Use the Nylatex Wrap to secure each
electrode in position on the patient.

LEAD WIRE SEATED

SECURE WITH
NYLATEX

RED +
LEAD WIRE

The Nylatex Wraps contain dry natural rubber and


may cause allergic reactions in patients with allergies
to latex.
BLACK
LEAD WIRE

38

PATIENT PREPARATION
ULTRASOUND PATIENT PREPARATION
Preparing Treatment Area
Examine the skin for any wounds and clean the skin.
Size of Applicator
View the Sound Head Recommendation in the Treatment
Review screen for Ultrasound (as a reference point only) prior to
administering treatment.
Sound Heads are available in the sizes shown below.
5 CM2
STANDARD
1 CM2

10 CM2

2 CM2

Intelect Advanced Therapy System

Conductive Medium
Liberally apply Conductor
Transmission Gel or equivalent to
the treatment area on the patient.

Treatment Area
Move the Sound Head during
therapy session in a circular
motion. The area treated should
be two times the diameter of the
Sound Head.

Applicator Coupling
If US Coupling is On, the Sound
Head is properly coupled to
the patient and administering
ultrasound when the LED is
constantly illuminated
Applicator Preparation
Clean applicator before each therapy session with warm soapy
water.

APPLY
CONDUCTIVE GEL

NOTE:
Refer to page 29 for US Coupling
settings.
39

COUPLING
INDICATOR
LED

OPERATION

Intelect Advanced Therapy System

OPERATOR INTERFACE
The Intelect Advanced Therapy System user Operator Interface houses all of the functions and controls necessary for the operator to
access all operator utilities, modalities, and parameters for modification and system set up.
1
8
8

2
3

5
7
6
12
9

11

10

1. Top of Screen
The Title Bar indicates the Screen Title
for the modality being used. When at
the System Home screen, the Clinic
Name is displayed.
2. Center of Screen
Contains available Modality options.
Select Modality by pressing the desired
Modality button and then make
parameter modifications.
3. Bottom of Screen
Displays available channels and their
respective status. Displays Treatment
Time and status. After starting therapy
session, Modality and Parameter buttons
are used to select and modify channel
parameters.
4. Unit On Indicator
Illuminates green when System is
connected to an AC mains power source.
When the System is On, the indicator
will illuminate blue. With System On,
and if the system sits unused, the Screen
Saver initiates (blank screen) and the Blue
Indicator will flash.
5. Back button
Used to return back one screen. Used in
conjunction with the Home button to
access the Operator Utilities screen.

40

6. Clinical Resources Library button


Used to access Clinical Protocols, User
Protocols, Sequencing, and the Clinical
(Anatomical/Pathological) Libraries
screen.
7. Home button
Used to go back to the System Home
screen. Used in conjunction with the
Back button to access the Operator
Utilities screen.
8. Modality and Parameter buttons
Used to select modality and edit
treatment parameters.
9. Intensity Knob
Rotate clockwise to increase Modality
intensity. Rotate counterclockwise to
decrease Modality intensity.
10. Start button
Press to start therapy session after all
initial parameters have been set.
11. Pause button
Press to pause a therapy session. Press
again to restart session.
12. Stop button
Press to completely stop the therapy
session.

OPERATION

Intelect Advanced Therapy System

HOME SCREEN
The Intelect Advanced Home screen affords access to all of the system modalities and functions. The area surrounding the screen has 10
modality and parameter modification buttons.
1. Electrotherapy
Accesses all the available waveforms and parameter editing controls.
2. Quick Link Indications
Accesses specific pre-programmed indications, for general reference only, which
aid in selecting the proper waveform and electrode placement for particular
1
2
indicated patient syndrome diagnoses.
Ultrasound
3.
3
4
Accesses the Ultrasound set up screen and parameter editing controls.
5
6
4. Combination
Accesses combination therapy set up screens and parameter editing controls.
7
8
5. sEMG*
9
10
Accesses the Surface EMG (sEMG) modality and parameter editing controls.
6. sEMG + Stim*
Accesses the Surface EMG (sEMG) + Electrical Stimulation modality and
parameter editing controls.
7. View/Edit Channel
Accesses the selected channel and allows editing of the channel's parameters
during therapy. Also used in the saving of information to the Patient Data Card.
8. Patient Card
Accesses Patient Data Card data.
Select Channel
9.
*NOTE:
Use to select desired channel for viewing and editing of channel parameters.
The sEMG Module is standard on the Intelect
10.
Unused
Advanced Therapy System Color Series and
Reserved for optional expansion Modules.
optional for the Monochromatic Series.
41

OPERATION

Intelect Advanced Therapy System

ELECTROTHERAPY SCREEN
The screen allows the operator to access, set up, and modify
parameters of each of the available waveforms within the
Intelect Advanced Therapy System. The following pages give a
general explanation of a treatment setup.
Refer to the Specifications section, beginning on page 15,
for detailed specifications of the system and each available
waveform.
NOTE:
Give patient the appropriate Patient Interrupt Switch for the
channels being used. Prior to starting a therapy session, explain
to the patient how to use the Patient Interrupt Switch.

42

OPERATION

Intelect Advanced Therapy System

GENERAL ELECTROTHERAPY WAVEFORM SET UP


The following information is an example of step by step set up for the Electrotherapy waveforms. All waveforms in the Intelect Advanced
Therapy System are set up and edited in the same basic fashion. The following set up instructions use IFC Traditional (4p) Waveform.
Prepare Patient
Refer to pages 35 through 38 for electrode
selection, preparing patient, and securing
electrodes.
Select Modality
Press the Electrotherapy button on the
Home screen.

Select Waveform
Press button beside the desired waveform
from the listing on the screen.
PRESS DESIRED WAVEFORM BUTTON

ELECTROTHERAPY
BUTTON

View Waveform Description


Press the Waveform Description button
to view text explaining the waveform
rationale.
WAVEFORM DESCRIPTION
BUTTON

NEXT
PAGE
BUTTON

BACK
BUTTON

Refer to Specifications section of this


manual for all available waveforms on the
Intelect Advanced Therapy System.

43

Press the Next Page button to view


additional text. Press the Back button to
return to the Treatment Review screen.

OPERATION

Intelect Advanced Therapy System

GENERAL ELECTROTHERAPY WAVEFORM SET UP (continued)


View Electrode Placement
Edit Waveform Parameters
Press the Electrode Placement button to
Press Edit button to access waveform
view the most commonly used electrode
parameters.
placement for the waveform selected.
Press the corresponding button to edit
each parameter as prescribed.
ELECTRODE PLACEMENT

Install Patient Interrupt Switch


Make certain the Patient Interrupt Switch is
connected to the Therapy System. Refer to
page 13 for Symbol Definitions.
LANYARD

BUTTON

EDIT
BUTTON

PARAMETER
BUTTONS

NEXT
PAGE
BUTTON

PATIENT
INTERRUPT
SWITCH

BACK
BUTTON
BACK
BUTTON

Press the Next button to read Electrode


Placement Text. Press the Back button to
return to the Treatment Review screen.

Press the Back button to return to the


Treatment Review screen.
44

NOTE:
When reinstalling the Front Access Panel,
make certain the Lanyard does not become
kinked.

OPERATION

Intelect Advanced Therapy System

GENERAL ELECTROTHERAPY WAVEFORM SET UP (continued)


Patient Interrupt Switch
Set Waveform Intensity
Give Patient Interrupt Switch to patient
and explain that pressing the Red button
once pauses the therapy session.

Set intensity by rotating the Intensity Control


Knob to the prescribed level.

PRESSING BUTTON ONCE PAUSES SESSION

Press the Start button to begin therapy


session.
START
BUTTON

INTENSITY
DISPLAYED

ROTATE
INTENSITY
KNOB

If Patient Interrupt Switch is depressed, the


treatment will be paused and a message
will appear on the System screen.
Press any button to clear the message.
NOTE:
If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.

Start Treatment

Intensity Knob Rotation


Clockwise- Increases Intensity
Counterclockwise- Decreases Intensity

45

OPERATION

Intelect Advanced Therapy System

GENERAL ELECTROTHERAPY WAVEFORM SET UP (continued)


Pause Treatment
Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

Stop Treatment
To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.
STOP BUTTON

PAUSE
BUTTON

46

Save to Patient Data Card


After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

OPERATION

Intelect Advanced Therapy System

ADJUSTING ELECTROTHERAPY CHANNEL PARAMETERS DURING TREATMENT


The Electrotherapy channel parameters may be changed during a treatment session without pausing or stopping the treatment. The
waveform Intensity may be increased or decreased at any time during the session without utilizing this process.
Select Channel
Press the Home button.

Press the Select Channel button until the


channel desired is framed.

Edit Channel Paramenters


Press the Edit button. Edit parameters as
desired.

VIEW/EDIT
BUTTON
EDIT
BUTTON

PARAMETER
BUTTONS

SELECT CHANNEL
BUTTON
DESIRED
CHANNEL
FRAMED

Press the View/Edit Channel button. The


Treatment Review screen will display.

47

When finished editing the selected


channel, press the Home button to select
another channel if desired.
To view the Treatment Review screen, if
the Home screen is displayed, press the
View/Edit Channel button. If the Edit
screen is displayed, press the Back button.

OPERATION

Intelect Advanced Therapy System

ULTRASOUND
The Intelect Advanced Therapy System Ultrasound modality allows the user to select specific Sound Head recommendations and edit
treatment parameters for various syndromes requiring the use of ultrasound therapy. The following information gives general instructions
for the setup of ultrasound therapy when selecting Ultrasound from the Home screen. Clinical Protocol and Quick Link Indication Ultrasound
treatment parameters are edited in the same basic fashion.
Prepare Patient
Refer to page 39 for Applicator sizes,
patient preparation, and use of conductive
medium.
NOTE:
Use only Intelect Advanced Ultrasound
Applicators. Previous models of
Chattanooga Group Ultrasound Applicators
will not work with the Intelect Advanced
Therapy System.

View Parameter Rationale


Press the Parameter Rationale button for
text. Press the Next Page button to continue
viewing text.
PARAMETER RATIONALE
BUTTON

Sound Head Recommendation


Press Sound Head Recommendation
button to view text explaining how to select
an Ultrasound Applicator size based on
treatment area.
SOUND HEAD
RECOMMENDATION
BUTTON

NEXT
PAGE
BUTTON

Select Modality
Press the Ultrasound button on the Home
screen.
ULTRASOUND
BUTTON

BACK
BUTTON

Press the Back button to the return to


Treatment Review screen.
48

BACK
BUTTON

Press the Back button to the return to


Treatment Review screen.

OPERATION

Intelect Advanced Therapy System

ULTRASOUND (continued)
Edit Ultrasound Parameters
Press Edit button to access ultrasound
parameters.
Press the corresponding button to edit as
prescribed.
EDIT
BUTTON

Head Warming
The Intelect Advanced Therapy System
incorporates a Head Warming feature that
pre-heats the Sound Head of the Applicator
for increasing patient comfort. The control
for the Head Warming feature is in the Edit
screen of the Ultrasound modality.
Press the Head Warming button until On is
displayed.

Set Ultrasound Intensity


Set intensity by rotating the Intensity Control
Knob to the prescribed level.

INTENSITY
DISPLAYED

HEAD WARMING
BUTTON
ROTATE
INTENSITY
KNOB

PARAMETER
BUTTONS

Press the Back button to return to


Treatment Review screen.

BACK
BUTTON

To set the default of the Head Warming


feature to On, press the Home button after
On is displayed in the Head Warming icon.
Head Warming will then start when the
Therapy System is turned On.
NOTE:
Head Warming time is approximately 2
minutes.
49

Intensity Knob Rotation


Clockwise- Increases Intensity
Counterclockwise- Decreases Intensity

OPERATION

Intelect Advanced Therapy System

ULTRASOUND (continued)
Start Treatment
Press the Start button to begin therapy
session.
Move the Applicator in a circular motion
over the treatment area.

START
BUTTON

Pause Treatment
Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.
or
If US Coupling is On, and the Sound
Head looses coupling with the treatment
area, the session will pause. When
coupling is reestablished, the session will
automatically restart. Refer to page 32 for
US Coupling settings.

Stop Treatment
To Stop treatment, press the Stop button
once. Treatment will stop and the
Treatment Review screen will display.
STOP BUTTON

PAUSE
BUTTON

Save to Patient Data Card


After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

NOTE:
If US Coupling is On and the Sound Head
looses coupling with the treatment area
the session will pause. When coupling is
reestablished the session will automatically
restart. See page 32 for US Coupling
settings.
50

OPERATION

Intelect Advanced Therapy System

ADJUSTING ULTRASOUND PARAMETERS DURING TREATMENT


The ultrasound parameters may be changed during a treatment session without pausing or stopping the treatment. The following
information provides instructions for changing ultrasound treatment parameters during a treatment session. The ultrasound intensity may be
increased or decreased at any time during the session without utilizing this process.
Editing Ultrasound from Home Screen
Editing Ultrasound from Treatment
Review Screen
Press the cooresponding parameter
Press Select Channel button until US:
button and edit as prescribed.
Running is framed.
Press the Edit button on the Treatment
Review screen.
Press View/Edit Channel button.
Press the cooresponding parameter
Press the Edit button on the Treatment
button and edit as prescribed.
Review screen.
EDIT
BUTTON

VIEW/EDIT
CHANNEL
BUTTON

SELECT
CHANNEL
BUTTON
US: RUNNING
FRAMED

BACK
BUTTON

PARAMETER
BUTTONS

PARAMETER
BUTTONS

EDIT
BUTTON

When editing is complete, press the Back


button to return to Treatment Review
screen
51

BACK
BUTTON

When editing is complete, press the Back


button to return to Treatment Review
screen.

OPERATION

Intelect Advanced Therapy System

QUICK LINK INDICATIONS


The Intelect Advanced Therapy System incorporates a unique Quick Link Indications section which allows the user to select specific Clinical
Indications and apply the most common therapy for the Indication selected. All modalities are editable, in their normal editing fashion, in
order to customize the treatment for each patients prescribed therapy.
Available Quick Link Indications

Select Quick Link Indication

Pain- (Acute, Subacute and Chronic)


Increase Local Circulation
Neuromuscular Re-education- (Spasticity,
Muscle Re-education and Stroke Muscle
Re-education)
Wound Healing- (Stage III and Stage IV)
Iontophoresis
Muscle Spasm
Edema- (Acute and Chronic)
Denervated Muscle- (Muscle Re-education
and S/D Curve)
Muscle Strengthening- (Phasic Muscle
Strengthening and Tonic Muscle Strengthening)
Waveforms- Link to Waveform and Current
Library. (Same as under Electrotherapy on Home
screen)
Prepare Patient
Refer to pages 35 through 38 for electrode
selection, preparing patient, and securing
electrodes.

Press the Quick Link Indications button on


the Home screen.
Press the corresponding button beside the
desired Quick Link Indication.

If prompted by the Therapy System, press


the corresponding button for the desired
Pathological Severity.
SELECT PATHOLOGICAL SEVERITY

QUICK LINK INDICATIONS BUTTON

PRESS
DESIRED
BUTTON

52

OPERATION

Intelect Advanced Therapy System

QUICK LINK INDICATIONS (continued)


View Waveform Description
Press the Waveform Description button
to view text explaining the waveform
rationale.
WAVEFORM DESCRIPTION
BUTTON

View Electrode Placement


Press the Electrode Placement button to
view the most commonly used electrode
placement for the waveform selected.
ELECTRODE PLACEMENT
BUTTON

Edit Waveform Parameters


Press Edit button to access waveform
parameters.
Press the corresponding button to edit
each parameter as prescribed.

EDIT
BUTTON
NEXT
PAGE
BUTTON

NEXT
PAGE
BUTTON

BACK
BUTTON

Press the Next Page button to view


additional text. Press the Back button to
return to the Treatment Review screen.

PARAMETER
BUTTONS

BACK
BUTTON

Press the Next button to read Electrode


Placement Text. Press the Back button to
return to the Treatment Review screen.

53

Press the Back button to return to the


Treatment Review screen

OPERATION
QUICK LINK INDICATIONS (continued)
Install Patient Interrupt Switch
Make certain the Patient Interrupt Switch is
connected to the unit. Refer to page 13 for
Symbol Definitions.
LANYARD

Intelect Advanced Therapy System

Patient Interrupt Switch


Give Patient Interrupt Switch to patient
and explain that pressing the Red button
once pauses the therapy session.

Reset intensity and press the Start button


to resume session.

PRESSING BUTTON ONCE PAUSES SESSION

START
BUTTON
PATIENT
INTERRUPT
SWITCH

NOTE:
When reinstalling the Front Access Panel,
make certain the Lanyard does not become
kinked.

If Patient Interrupt Switch is depressed, the


treatment will be paused and a message
will appear on the System screen.
Press any button to clear the message.
NOTE:
If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.
54

OPERATION

Intelect Advanced Therapy System

QUICK LINK INDICATIONS (continued


Setting Waveform Intensity
Set intensity by rotating the Intensity Control
Knob to the prescribed level.

Start Treatment
Press the Start button to begin therapy
session.
START
BUTTON

Pause Treatment
Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.
PAUSE
BUTTON

INTENSITY
DISPLAYED

ROTATE
INTENSITY
KNOB

Intensity Knob Rotation


Clockwise- Increases Intensity
Counterclockwise- Decreases Intensity

55

OPERATION

Intelect Advanced Therapy System

QUICK LINK INDICATIONS (continued)


Stop Treatment
To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.
STOP BUTTON

Editing Parameters during Treatment


Session
The parameters may be edited during
a treatment session without pausing or
stopping the treatment.
Refer to page 47 for parameter changes
to electrotherapy waveforms and currents
and page 51 for editing Ultrasound.
NOTE:
The intensity can be increased or decreased
by rotating the Intensity Knob as desired
without pressing the Edit button.

56

Save to Patient Data Card


After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

OPERATION

Intelect Advanced Therapy System

COMBINATION
The Intelect Advanced Therapy System Combination modality allows the user to select and use ultrasound therapy in combination with
electrical muscle stimulation.
Combination therapy utilizes the Ultrasound modality in conjuction with High Voltage Pulsed Current (HVPC), IFC (4p), IFC (2p), Asymmetrical
Biphasic, Symmetrical Biphasic, or VMSTM to generate a therapeutic effect. In this mode of therapy, the Sound Head of the Ultrasound
Applicator becomes one half of the electrical circuit. An electrode attached to the Red (+) Lead Wire completes the circuit.
Prepare Patient
Refer to pages 35 through 38 to prepare
patient, select electrode, and securing
electrodes. Refer to page 39 for Ultrasound
patient preparation.
Connect the Black (-) Lead Wire from
Channel 2 to the electrode. Make certain
the Lead Wire is completely seated in the
electrode.
The Red (+) Lead Wire is not used. The
Ultrasound Applicator completes the
circuit for Combination Therapy.

Select Modality
Press the Combination button on the Home
screen.
COMBINATION
BUTTON

View Application Description


Press the Waveform Description button
to view text explaining the waveform
rationale.
APPLICATION
DESCRIPTION
BUTTON

BACK
BUTTON

Press the Back button to return to the


Treatment Review screen.

57

OPERATION

Intelect Advanced Therapy System

COMBINATION (continued)
View Electrode Placement
Press the Electrode Placement button to
view the most commonly used electrode
placement for Combination therapy.

Access Combination Parameters


Press Edit button to access Combination
parameters.

ELECTRODE PLACEMENT
BUTTON

Edit Ultrasound Parameters


Press the corresponding button to edit
the desired Ultrasound parameter as
prescribed.
PARAMETER
BUTTONS

EDIT
BUTTON
NEXT
PAGE
BUTTON

BACK
BUTTON

Press the Next button to read Electrode


Placement Text. Press the Back button to
return to the Treatment Review screen.
Press the Back button to return to the
Treatment Review screen.

58

NOTE:
See page 49 for Head Warming feature
instructions.

OPERATION

Intelect Advanced Therapy System

COMBINATION (continued)
Select Waveform
Press the Select Waveform button.
SELECT WAVEFORM
BUTTON

UP ARROW
BUTTON

Patient Interrupt Switch


Connect Patient Interrupt Switch to the
Therapy System. Give Patient Interrupt
Switch to patient and explain that pressing
the Red button once pauses the therapy
session.
CONNECT PATIENT
INTERRUPT SWITCH

ACCEPT AND
RETUN ARROW
BUTTON

Press the Up or Down Arrow buttons until


the prescribed waveform is highlighted.
Press the Accept and Return Arrow button.

EDIT STIM
BUTTON
PARAMETER
BUTTONS

PATIENT INTERRUPT
SWITCH

DOWN ARROW
BUTTON

Edit Waveform Parameters


Press the Edit Stim button to edit the
parameters of the waveform selected.
Press the corresponding button to edit
each parameter as prescribed.

If Patient Interrupt Switch is depressed, the


treatment will be paused and a message
will appear on the System screen.
Press any button to clear the message.
NOTE:
If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.
59

OPERATION

Intelect Advanced Therapy System

COMBINATION (continued)
Set Waveform Intensity

Set Ultrasound Intensity

Set intensity by rotating the Intensity Control


Knob to the prescribed level.

Press the Edit Ultrasound button.


Set Ultrasound intensity by rotating the
Intensity Control Knob to the prescribed level.
EDIT
ULTRASOUND
BUTTON

INTENSITY
DISPLAYED

Press the Start button to begin therapy


session.
Move the Applicator in a circular motion
on the treatment area.
START
BUTTON

ROTATE
INTENSITY
KNOB

Intensity Knob Rotation


Clockwise- Increases Intensity
Counterclockwise- Decreases Intensity

Start Treatment

ROTATE
INTENSITY
KNOB

Intensity Knob Rotation


Clockwise- Increases Intensity
Counterclockwise- Decreases Intensity

60

NOTE:
If US Coupling is On and the Sound
Head looses coupling with the treatment
area the session will pause. When
coupling is reestablished, the session will
automatically restart. See page 32 for US
Coupling settings.

OPERATION

Intelect Advanced Therapy System

COMBINATION (continued)
Pause Treatment
Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

Stop Treatment
To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.
STOP BUTTON

PAUSE
BUTTON

61

Save to Patient Data Card


After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

OPERATION

Intelect Advanced Therapy System

ADJUSTING COMBINATION PARAMETERS DURING TREATMENT


The channel parameters may be changed during a treatment session without pausing or stopping the treatment. The following information
provides instructions for changing Combination Treatment Electrotherapy Channel and Ultrasound parameters during a treatment session.
Edit Waveform Parameters
Press the Edit Stim button to edit the
parameters of the waveform selected.
Press the corresponding button to edit
each parameter as prescribed.
Rotate the Intensity Knob to increase or
decrease waveform intensity as prescribed.

Edit Ultrasound Parameters


Press the Edit Ultrasound button.
Press the corresponding button to edit
the desired Ultrasound parameter as
prescribed.
EDIT
ULTRASOUND
BUTTON

PARAMETER
BUTTONS

EDIT STIM
BUTTON
PARAMETER
BUTTONS

NOTE:
See page 49 for Head Warming feature
instructions.
62

NOTE:
To edit parameters from the Home
screen, see page 47 for selecting channel
instructions.

OPERATION

Intelect Advanced Therapy System

PATIENT DATA CARD SET UP OF NEW CARD


General Information
The Intelect Advanced Therapy System incorporates a Patient Data Card reading and recording device that allows transfer of patient therapy
data from the system to the card for reviewing patient modality and pain profile information. Information may be transferred to a PC via the
optional Patient Data Management System. The PC software is designed to allow easy access to patient data and printing of reports as well as
adding session notes to the Patient Data Card.
The reading and recording device allows storage and recall of the following patient session data onto the Patient Data Card: therapy session
parameters, Electrode Placement, Pain Map, Numeric Pain Scale or Visual Pain Scale, and Session Notes (stored on card via PC only). Each
Patient Data Card can store multiple sessions and each session can be recalled on the Intelect Advanced Therapy System.
Insert New Patient Data Card
Insert a new Patient Data Card into the
system access port as shown below. The
Therapy System will automatically format
the new Patient Data Card and a verification
message will appear.
Press any button to continue.

Setup Treatment
Set up the patient's prescribed treatment.
Refer to the appropriate area of this manual
for modality set up.
Administer treatment as prescribed. When
treatment is complete, the Treatment
Review screen will be visible.

INSERT NEW
PATIENT DATA CARD

PRESS ANY BUTTON


TO CONTINUE

63

Set Up of New Patient Data Card


With new Patient Data Card inserted in
the system, press the Save to Patient Card
button.
SAVE TO
PATIENT CARD
BUTTON

OPERATION

Intelect Advanced Therapy System

PATIENT DATA CARD SET UP OF NEW CARD (continued)


Enter Patient ID
Select the row of alpha or numeric
characters desired by pushing the button
beside the corresponding row. Select the
desired character in the row by pressing
the row button until the desired letter is
framed.
SELECT ROW AND CHARACTERS

When the desired character is framed, press


the Accept and Return Arrow button. The
character selected will display in the top of
the screen and the cursor will advance to
the next position.
To move back a character, press the Left
Arrow button.
CHARACTER
DISPLAYED

To discard entire entry, press the Back


button.
Repeat this procedure until the desired
Patient ID is entered.
After Patient ID is entered, press the Save
button.

SAVE
BUTTON

ACCEPT AND RETURN


ARROW BUTTON

LEFT
ARROW
BUTTON

To delete a character, press the Left Arrow


button until the character to be deleted is
framed. Press the Delete button.
64

OPERATION

Intelect Advanced Therapy System

PATIENT DATA CARD SET UP OF NEW CARD (continued)


Electrode Placement Set Up
Access Electrode Placement
Press the Pad button to select the Red (+) or
The following information uses the IFC
Black (-) electrode.
Traditional (4p) as an example. Electrode
Placement procedures for all modalities are
Press the Chan button to select (1) or
performed in the same basic fashion.
Channel B (2).
Press the Electrode Placement button.
Press the Side button to select Front, Back,
ELECTRODE PLACEMENT BUTTON

Left, or Right of the body graphic.


Press the Size button until desired electrode
size is displayed. If electrode desired is not
listed, select Other.
PAD
BUTTON

Electrode Placement
Press the Up, Down, Left and Right Arrow
buttons to position the selected electrode
as close to the actual treatment location as
possible.
Press the Pad button to select the other
electrode. Repeat above procedure for
electrode positioning.
If applicable, press the Chan button, to
select another channel and repeat above
procedures.
After positioning the electrodes, press the
Accept and Return Arrow button.

CHAN
BUTTON

ELECTRODES
POSITIONED

SIDE
BUTTON
SIZE
BUTTON

NOTE:
When Ultrasound is the modality, only the
Side button is available.
65

ACCEPT AND RETURN


ARROW BUTTON

OPERATION

Intelect Advanced Therapy System

PATIENT DATA CARD SET UP OF NEW CARD (continued)


Access Pain Map
Press the Pain Map button to select
the body area of the associated pain as
described by the patient.

Select Pain Type


Press the Pain Type button until the
desired description is displayed in the Pain
Type icon.

PAIN MAP BUTTON


PAIN TYPE
BUTTON

66

Add Pain Locations


Press the Add button. The Add Pain Map
window will display.
ADD
BUTTON

OPERATION

Intelect Advanced Therapy System

PATIENT DATA CARD SET UP OF NEW CARD (continued)


Select Location of Pain
Press the Up and Down Arrow buttons to
move the Pain Locator to the area of the
body where the pain originates.
Press the Accept and Return Arrow button.
The Pain Map window will display.
PAIN
LOCATOR

UP AND DOWN
ARROW BUTTONS

Press the Add button to continue selecting,


in sequence, the radiating path of the pain
using the above procedure.
Up to eight pain locations may be selected.

Editing Pain Locations


Press the Edit button on the Pain Map
window.
EDIT
BUTTON

ADD
BUTTON

UP AND DOWN
ARROW BUTTONS

EDIT NEXT
BUTTON
ACCEPT AND RETURN
ARROW BUTTON
BACK
BUTTON

ACCEPT AND RETURN


ARROW BUTTON

After all desired Pain Locations have been


made, press the Back button.
67

Press the Edit Next button to highlight the


Pain Location to be edited.
Use the Up and Down Arrow buttons to
relocate the selected Pain Location.
Press the Accept and Return Arrow button.
Repeat until all editing is complete, then
press the Back button.

OPERATION

Intelect Advanced Therapy System

PATIENT DATA CARD SET UP OF NEW CARD (continued)


Deleting Pain Locations
Press the Delete button on the Pain Map
window
DELETE
BUTTON
UP AND DOWN
ARROW BUTTONS

Pain Scales
The Intelect Advanced Therapy System incorporates two internationally recognized Pain
Scales; VAS Visual Analog Scale, Scale has no indicator marks or Numeric (indicated 1
through 10) for use in describing the amount of pain the patient is experiencing. Once one
of the pain scales is set, the other will automatically set to the corresponding level.
Select Pain Scale
Adjust Pain Scale
Select the desired Pain Scale by pressing the
Press the Left and Right Arrow buttons to
corresponding button.
adjust the Pain Scale to the level the patient
is experiencing.
NUMERIC PAIN
SCALE BUTTON

LEFT
ARROW
BUTTON

RIGHT
ARROW
BUTTON

DELETE
BUTTON
ACCEPT AND RETURN
ARROW BUTTON
VISUAL PAIN
SCALE BUTTON

Use the Up and Down Arrow buttons to


highlight the Pain Location to be deleted.
Press the Delete button.
Press the Accept and Return Arrow button.
Repeat until all editing is complete, then
press the Back button.

ACCEPT AND RETURN


ARROW BUTTON

After the desired level is achieved, press the


Accept and Return Arrow button.
NOTE:
Numeric Pain Scale illustrated.
68

OPERATION

Intelect Advanced Therapy System

PATIENT DATA CARD SET UP OF NEW CARD (continued)


Save to Patient Data Card
After all desired session data has been
entered in the Patient Data Card screens,
press the Save to Patient Card button. A
message will appear stating the data has
been saved to the Patient Data Card.
Press any button.

the Home button.


Remove the Patient Data Card for filing with
patient records.
The Patient Data Card can also be used with
the optional Patient Data Management
System.

SAVE TO PATIENT
CARD BUTTON

After pressing any button, the Completed


Treatment Review screen will display. Press

69

OPERATION
EXISTING PATIENT DATA CARD USE
Insert Existing Patient Data Card
Insert the Patient Data Card assigned to the
patient receiving treatment into the system
access port as shown below.
INSERT EXISTING
PATIENT DATA CARD

Intelect Advanced Therapy System

Access Patient Data Card


Press the Patient Card button to access
Patient Data Card.
Select the date of the treatment session
desired using the Up and Down Arrow
buttons until date desired is highlighted.

View Patient Data Card


Press the corresponding button beside the
Patient Data to be viewed.

PATIENT CARD
BUTTON
UP ARROW
BUTTON

DOWN ARROW
BUTTON

70

NOTE:
No Session Notes will be available unless
the optional Patient Data Management
System was utilized to enter Session Notes
onto the Patient Data Card.

OPERATION

Intelect Advanced Therapy System

EXISTING PATIENT DATA CARD USE (continued)


Starting a New Treatment from Patient
Patient Interrupt Switch
Data Card
Connect Patient Interrupt Switch to the
Therapy System. Give Patient Interrupt
Refer to pages 35-38 for Electrotherapy
Switch to patient and explain that pressing
patient preparation, select electrodes, and
the Red button once pauses the therapy
secure electrodes. Refer to page 39 for
session.
Ultrasound patient preparation.
CONNECT PATIENT
Press the Up and Down Arrow buttons to
INTERRUPT SWITCH
highlight the desired treatment date and
time.
Press the View Treat. button.
PATIENT
INTERRUPT
Press Start New Treatment button.
SWITCH

VIEW TREAT.
BUTTON

Set Intensity
Set intensity by rotating the Intensity Control
Knob to the prescribed level.

INTENSITY
DISPLAYED

ROTATE
INTENSITY
KNOB

START NEW
TREATMENT
BUTTON

If Patient Interrupt Switch is depressed, the


treatment will be paused and a message
will appear on the System screen.
Press any button to clear the message.
NOTE:
If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.
71

Intensity Knob Rotation


Clockwise- Increases Intensity
Counterclockwise- Decreases Intensity

OPERATION

Intelect Advanced Therapy System

EXISTING PATIENT DATA CARD USE (continued)


Start Treatment
Press the Start button to begin therapy
session.
START
BUTTON

Pause Treatment
Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

Stop Treatment
To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.
STOP BUTTON

PAUSE
BUTTON

Erasing Patient Data Card


Refer to page 31 for proper Patient Data
Card Erasing instructions.

72

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY CLINICAL PROTOCOLS


The Intelect Advanced Clinical Resources Library contains Clinical Protocols, User Protocols, Sequencing functions and access to the
Multimedia Card (MMC) which contains the Anatomical and Pathological Libraries.
Clinical Protocols
This library is a series of protocol presets where the Body Area, Clinical Indication, Pathological Condition, and Pathological Severity are
selected by the user, and the Clinical Protocols algorithm will select the parameter settings. These Clinical Protocols are to be used only as
guidelines. Each patient should be individually assessed to determine the appropriateness of the protocol parameters prior to use. All
Clinical Protocols can be edited to suit appropriate patient treatment prescription and patient comfort.
The following information gives general instructions to access, selection and setup of Clinical Protocols. Each Clinical Protocol is set up and
edited in the same basic manner.
Access Clinical Resources
Press the Clinical Resources Library button.
CLINICAL RESOURCES
LIBRARY BUTTON

Access Clinical Protocols


Press the Clinical Protocols button.
CLINICAL
PROTOCOLS
BUTTON

Select Body Area


Press the button corresponding to the
body area desired.
BODY AREA BUTTONS

73

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY CLINICAL PROTOCOLS (continued)


Select Clinical Indication
Press the button beside the Clinical
Indication desired in either the
Electrotherapy or Ultrasound screen
section.

Select Pathological Condition


Press the button beside the desired
Pathological Condition.
PATHOLOGICAL CONDITION BUTTONS

Select Pathological Severity


Press the button beside the desired
Pathological Condition.
PATHOLOGICAL SEVERITY BUTTONS

CLINICAL INDICATION BUTTONS

NOTE:
Not all Pathological Conditions have
corresponding Pathological Severity
windows. Some go directly to the
associated modality Treatment Review
screen.

74

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY CLINICAL PROTOCOLS (continued)


View Waveform Rationale
Press the Waveform Rationale button
(Electrotherapy Modalities) or the Parameter
Rationale (Ultrasound Modality) to view
the text explaining the rationale for the
modality associated with the specific
Clinical Protocol selected.

View Electrode Placement


Press the Electrode Placement button to
view the specific electrode placement for
the Clinical Protocol selected.
ELECTRODE PLACEMENT
BUTTON
NEXT PAGE
BUTTON

WAVEFORM RATIONALE
BUTTON

BACK
BUTTON
BACK
BUTTON

Press the Back button to return to the


Treatment Review screen.

Press the Next Page button to view text


relating to the electrode placement.
Press the Back button to return to the
Treatment Review screen.

75

Prepare Patient
Refer to pages 35 through 38 for
Electrotherapy and page 39 Ultrasound
patient preparation instructions. For sEMG
and sEMG+Stim patient Preparation, refer
to the sEMG and sEMG+Stim Module User
Manual.
Edit Modality Parameters
Press the Edit button.
Edit modality parameters as prescribed.
Refer to page 44 for Electrotherapy
modalities and page 49 for Ultrasound.
Refer to the sEMG and sEMG+Stim Module
User Manual for sEMG and sEMG+Stim
modalities.
EDIT
BUTTON

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY CLINICAL PROTOCOLS (continued)


Patient Interrupt Switch
Make certain the Patient Interrupt Switch,
for the channel(s) being used, is connected
to the Therapy System. Refer to page 13 for
Symbol Definitions.

Give Patient Interrupt Switch to patient


and explain that pressing the Red button
once pauses the therapy session.

Set Modality Intensity


Set intensity by rotating the Intensity Control
Knob to the prescribed level.

PRESSING BUTTON ONCE PAUSES SESSION


LANYARD
INTENSITY
DISPLAYED

PATIENT
INTERRUPT
SWITCH

NOTE:
When reinstalling the Front Access Panel,
make certain the Lanyard does not become
kinked.

ROTATE
INTENSITY
KNOB

If Patient Interrupt Switch is depressed, the


treatment will be paused and a message
will appear on the System screen.
Press any button to clear the message.
NOTE:
If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.
76

Intensity Knob Rotation


Clockwise- Increases Intensity
Counterclockwise- Decreases Intensity

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY CLINICAL PROTOCOLS (continued)


Start Treatment
Press the Start button to begin therapy
session.
START
BUTTON

Pause Treatment
Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

Stop Treatment
To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.
STOP BUTTON

PAUSE
BUTTON

NOTE:
Modality parameters may be editied at any
time during the therapy session. Refer to
page 47 for Electrotherapy and page 51 for
Ultrasound.

Save to Patient Data Card


After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

77

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY CREATING USER PROTOCOLS


General Information
This library is a series of protocols created by the user and stored in the system memory. The following information gives general instructions
as to setting up, saving and accessing User Protocols. Should the Default Protocols be restored, through the User Utilities, all User Protocols will
be permanently removed from the system.
The Therapy System memory will accommodate up to 200 user defined protocols. This is inclusive of all User Protocols, User Sequences and
System Default Protocols. It does not include the Clinical Protocols.
Select Modality
Press the button beside the desired
modality on the Home screen or select
a Clinical Protocol using the Clinical
Resources Library button.
MODALITY BUTTONS

Edit Modality Parameters


Press the modality Edit button (usually
in the lower right corner of the modality
Treatment Review screen) and edit as
prescribed.
Refer to respective sections of this manual
for Electrotherapy, Quick Link Indications
Ultrasound, and Combination modalities.
For sEMG and sEMG+Stim modalities, refer
to the sEMG and sEMG+Stim Module User
Manual.

CLINICAL RESOURCES
LIBRARY BUTTON
EDIT
BUTTON

78

Select Clinical Resources Library


Press the Clinical Resources Library button
to begin the save process of the new User
Protocol.

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY CREATING USER PROTOCOLS (continued)


Enter User Protocol Name
Select the row of alpha or numeric
characters desired by pushing the button
beside the corresponding row. Select the
desired character in the row by pressing
the row button until the desired letter is
framed.
SELECT ROW AND CHARACTERS

When the desired character is framed, press


the Accept and Return Arrow button. The
character selected will display in the top of
the screen and the cursor will advance to
the next position.
To move back a character, press the Left
Arrow button.

To discard entire entry, press the Back


button.
Repeat this procedure until the desired User
Protocol Name is entered.
After User Protocol Name is entered, press
the Save button.

CHARACTER
DISPLAYED
SAVE
BUTTON

ACCEPT AND RETURN


ARROW BUTTON

LEFT
ARROW
BUTTON

To delete a character, press the Left Arrow


button until the character to be deleted is
framed. Press the Delete button.
79

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY DELETING USER PROTOCOLS


General Information
The following information provides instructions for the deletion of one User Protocol at a time. Once any single User Protocol is deleted, it
cannot be recovered. Should the Default Protocols be restored, through the User Utilities, all User Protocols will be permanently removed from
the system.
There is no method for recovery of the User Protocols nor can they be saved to any other medium.
Select Clinical Resources Library
Press the Clinical Resources Library button.
Then press the User Protocols button.

Select User Protocol to Delete


Press the UP and Down Arrow buttons until the
desired User Protocol to delete is highlighted.
UP AND DOWN
ARROW BUTTONS

Delete User Protocol


Press the Delete button to delete highlighted
User Protocol.
A verification screen will appear. Press Yes
button to delete protocol or No button to keep
protocol.

DELETE
BUTTON
NO
BUTTON

YES
BUTTON

Repeat this process until all desired User


Protocols are deleted.
Press the Home button to return to the Home
screen.

USER
PROTOCOLS
BUTTON

80

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY USING USER PROTOCOLS


Access User Protocols
Press the Clinical Resources Library button.
Press the User Protocols button.

Select User Protocol


Press the UP and Down Arrow buttons until the
prescribed User Protocol is highlighted.
Press the Accept and Return Arrow button.
UP ARROW
BUTTON

View Waveform Rationale


Press the Waveform Rationale button
(Electrotherapy Modalities) or the Parameter
Rationale (Ultrasound Modality) button
to view the text explaining the rationale
for the modality associated with the User
Protocol selected.
WAVEFORM RATIONALE
BUTTON

USER
PROTOCOLS
BUTTON

ACCEPT AND
RETURN ARROW
BUTTON

DOWN ARROW
BUTTON

BACK
BUTTON

Press the Back button to return to the


Treatment Review screen.

81

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY USING USER PROTOCOLS (continued)


View Electrode Placement
Prepare Patient
Press the Electrode Placement button to
Refer to pages 35 through 38 for
view the electrode placement for the User
Electrotherapy and page 39 for Ultrasound
Protocol selected.
patient preparation instructions. For sEMG
and sEMG+Stim patient preparation, refer
ELECTRODE PLACEMENT
to the sEMG and sEMG+Stim Module User
BUTTON
Manual.
NEXT PAGE
BUTTON

Edit Modality Parameters


Press the Edit button.
Edit modality parameters as prescribed.
Refer to page 44 for Electrotherapy
modalities and page 49 for Ultrasound.
Refer to the sEMG and sEMG+Stim Module
User Manual for sEMG and sEMG+Stim
modalities.

Patient Interrupt Switch


Make certain the Patient Interrupt Switch,
for the channel(s) being used, is connected
to the Therapy System. Refer to page 13 for
Symbol Definitions.
LANYARD

PATIENT
INTERRUPT
SWITCH

BACK
BUTTON
EDIT
BUTTON

NOTE:
When reinstalling the Front Access Panel,
make certain the Lanyard does not become
kinked.

Press the Next Page button to view text


relating to the electrode placement.
Press the Back button to return to the
Treatment Review screen.

82

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY USING USER PROTOCOLS (continued)


Give Patient Interrupt Switch to patient
and explain that pressing the Red button
once pauses the therapy session.

Set Modality Intensity


Set intensity by rotating the Intensity Control
Knob to the prescribed level.

Start Treatment
Press the Start button to begin therapy
session.
START
BUTTON

PRESSING BUTTON ONCE PAUSES SESSION

INTENSITY
DISPLAYED
ROTATE
INTENSITY
KNOB

If Patient Interrupt Switch is depressed, the


treatment will be paused and a message
will appear on the System screen.
Press any button to clear the message.
NOTE:
If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.

Intensity Knob Rotation


Clockwise- Increases Intensity
Counterclockwise- Decreases Intensity

83

NOTE:
Modality parameters may be edited at any
time during the therapy session. Refer to
page 47 for Electrotherapy and page 51 for
Ultrasound.

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY USING USER PROTOCOLS (continued)


Pause Treatment
Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

Stop Treatment
To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.
STOP BUTTON

PAUSE
BUTTON

84

Save to Patient Data Card


After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY CREATING NEW SEQUENCES


General Information
This Library is a series of Electrotherapy Waveform/Current Sequences created by the user for special electrotherapy treatment purposes and
stored in the system memory for recall and use. The following information gives general instructions for setting up, saving and accessing of
sequences. Should the Default Protocols be restored, through the User Utilities, all user saved Sequences will be permanently removed from
the system.
The Therapy System memory will accommodate up to 200 user defined protocols. This is inclusive of all User Protocols, Sequences, and
System Default Protocols. It does not include the Clinical Protocols.
Access Sequencing
Press the Clinical Resources Library button.
Press the Sequencing button.

Select Sequence
Press the Up and Down Arrow buttons until
the desired sequence is highlighted.
Press the Accept and Return Arrow button.

Select First Waveform or Current


Press the New button. Press the Up and
Down Arrow buttons to highlight the
desired waveform/current.

UP ARROW
BUTTON

NEW
BUTTON

SEQUENCING
BUTTON

UP ARROW
BUTTON

ACCEPT AND
RETURN ARROW
BUTTON

DOWN ARROW
BUTTON

ACCEPT AND RETURN


ARROW BUTTON

DOWN
ARROW
BUTTON

Press the Accept and Return Arrow button.


85

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY CREATING NEW SEQUENCES (continued)


Edit First Waveform or Current
Press the Edit button on the Sequence
screen.
Press the Edit button on the waveform/
current Treatment Review screen.

Select Second Waveform or Current


Press the Down Arrow button on the
Sequence screen to highlight the next
waveform in the Sequence.

DOWN
ARROW
BUTTON

EDIT
BUTTON

EDIT
BUTTON

Repeat steps used in selecting and editing


first waveform/current for second and third
waveform/current.

Edit waveform or current as prescribed.


Press the Back button twice to go back to
the Sequence screen.

86

Saving New Sequence


After all waveforms/currents have been
selected and edited as prescribed, press the
Save button on the Sequence screen.

SAVE
BUTTON

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY CREATING NEW SEQUENCES (continued)


Enter Sequence Name
Select the row of alpha or numeric
characters desired by pushing the button
beside the corresponding row. Select the
desired character in the row by pressing
the row button until the desired letter is
framed.
SELECT ROW AND CHARACTERS

When the desired character is framed, press


the Accept and Return Arrow button. The
character selected will display in the top of
the screen and the cursor will advance to
the next position.
To move back a character, press the Left
Arrow button.

To discard entire entry, press the Back


button.
Repeat this procedure until the desired
sequence name is entered.
After sequence name is entered, press the
Save button.

CHARACTER
DISPLAYED
SAVE
BUTTON

ACCEPT AND RETURN


ARROW BUTTON

LEFT
ARROW
BUTTON

To delete a character, press the Left Arrow


button until the character to be deleted is
framed. Press the Delete button.
87

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY DELETING SEQUENCES


General Information
The following information provides instructions for the deletion of one user defined sequence at a time. Once any single sequence is deleted,
it cannot be recovered. Should the Default Protocols be restored, through the User Utilities, all user defined sequences will be permanently
removed from the system.
There is no method for recovery of the user defined Sequences nor can they be saved to any other medium. There are nine Default
Sequences, indicated by an asterisk(*), that cannot be deleted.
Access Sequencing
Press the Clinical Resources Library button.
Press the Sequencing button.

Select Sequence
Press the Up and Down Arrow buttons until
the desired Sequence is highlighted.
UP AND DOWN
ARROW BUTTONS

Delete Sequence
Press the Delete button to delete highlighted
Sequence.
A verification screen will appear. Press Yes button
to delete Sequence or No button to keep
Sequence.

SEQUENCING
BUTTON
DELETE
BUTTON
NO
BUTTON

YES
BUTTON

Repeat this process until all desired user defined


Sequences are deleted.
Press the Home button to return to the Home
screen.
88

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY USING SEQUENCES


Access Sequencing
Press the Clinical Resources Library button.
Press the Sequencing button.

Select Sequence
Press the UP and Down Arrow buttons until the
prescribed Sequence is highlighted.
Press the Accept and Return Arrow button.
UP ARROW
BUTTON

Select Waveform/Current
Press the Down Arrow button, on the
Sequence screen, to highlight the
prescribed waveform/current in the
Sequence.
Press the Edit button.
DOWN
ARROW
BUTTON
EDIT
BUTTON

ACCEPT AND
RETURN ARROW
BUTTON
SEQUENCING
BUTTON

89

DOWN ARROW
BUTTON

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY USING SEQUENCES (continued)


View Waveform Rationale
Press the Waveform Description button to
view the text explaining the rationale for
the modality associated with the Sequence
selected.
WAVEFORM RATIONALE
BUTTON

View Electrode Placement


Press the Electrode Placement button
to view the electrode placement for the
Sequence selected.
ELECTRODE PLACEMENT
BUTTON

NEXT PAGE
BUTTON

Prepare Patient
Refer to pages 35 through 38 for
Electrotherapy patient preparation
instructions.
Patient Interrupt Switch
Make certain the Patient Interrupt Switch,
for the channel(s) being used, is connected
to the Therapy System. Refer to page 13 for
Symbol Definitions.
LANYARD

PATIENT
INTERRUPT
SWITCH
BACK
BUTTON

BACK
BUTTON

Press the Back button twice to return to the


Sequence screen.

Press the Next Page button to view text


relating to the electrode placement.
Press the Back button twice to return to the
Sequence screen.

90

NOTE:
When reinstalling the Front Access Panel,
make certain the Lanyard does not become
kinked.

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY USING SEQUENCES (continued)


Give Patient Interrupt Switch to patient
and explain that pressing the Red button
once pauses the therapy session.

Set Sequence Intensity


The first waveform/current in the Sequence
should be highlighted. Set intensity by
rotating the Intensity Control Knob to the
prescribed level.

PRESSING BUTTON ONCE PAUSES SESSION

Press the Down Arrow button until the


second waveform/current in the sequence is
Highlighted.
Set intensity by rotating the Intensity Control
Knob to the prescribed level.
DOWN
ARROW
BUTTON

If Patient Interrupt Switch is depressed, the


treatment will be paused and a message
will appear on the System screen.
Press any button to clear the message.
NOTE:
If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.

INTENSITY DISPLAYED

Intensity Knob Rotation


Clockwise- Increases Intensity
Counterclockwise- Decreases Intensity
91

Repeat for the third waveform/current in the


Sequence.

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY USING SEQUENCES (continued)


Start Treatment
Press the Start button to begin therapy
session.
START
BUTTON

Pause Treatment
Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

Stop Treatment
To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.
STOP BUTTON

PAUSE
BUTTON

Save to Patient Data Card


After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

92

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY MMC GRAPHICAL LIBRARY


General Information
The Clinical Resources Library contains the unique Anatomical and Pathological Graphic Libraries* from Chattanooga Group. These Graphic
Libraries are contained on a single Multimedia Card (MMC) and are designed to aid the operator in visually understanding and locating
specific muscle groups and commonly found problems associated with Pathological Conditions as well as providing an educational tool for
the clinician to use with the patient.
Select Clinincal Resources Library
Make certain the Multimedia Card (MMC) is
inserted into the system MMC Access Port.
Press the Clinical Resources Library button.

Select MMC Graphical Library


Press the MMC Graphical Library button.

Select Body Area


The default setting displays Upper Body
Selections. To view Lower Body Selections,
press the Lower Body button.
Press the button beside the desired Body
Area.
BODY AREA SELECTION BUTTONS

MMC
CARD

LOWER BODY
BUTTON

NOTE:
For representation purposes the Shoulder
has been selected for this section.

*Copyright 2003 Nucleus Medical Art. All rights reserved.


www.nucleusinc.com

93

OPERATION

Intelect Advanced Therapy System

CLINICAL RESOURCES LIBRARY MMC GRAPHICAL LIBRARY (continued)


Select Library Type
Anatomical Example- Muscles
Select the desired graphic by pressing the
Superficial
corresponding button.
Left Side buttons- Anatomical Selections
Right Side buttons- Pathological
Selections
ANATOMICAL
SELECTIONS

Pathological Example- Rotator Cuff Tear

PATHOLOGICAL
SELECTIONS

Press the Back button to return to the


selection screen.
Press the Home button to return to the
Home screen.
94

Press the Back button to return to the


selection screen.
Press the Home button to return to the
Home screen.

INSTALLATION/REMOVAL

Intelect Advanced Therapy System

INSTALLATION CHANNEL 3/4 ELECTROTHERAPY MODULE


General Information
The Intelect Advanced Therapy System Channel 3/4 Electrotherapy Module is a two channel electrotherapy module intended to upgrade
the Intelect Advanced Therapy System Two Channel Electrotherapy and Two Channel Combination Therapy Systems to Four Channel
Electrotherapy or Combination Therapy Systems. This module is designed for use with the Intelect Advanced Therapy Systems only.
Read, understand, and follow all precautionary instructions found on pages 2 through 6, and throughout this manual as indicated,
before performing any installation or removal of optional modules and accessories.
Perform all optional module and accessory installation and removal procedures as described in this manual. Failure to follow these
explicit instructions could cause permanent damage to internal components of the equipment and render the system unsafe for
patient therapy.
Understand all symbols and their definitions before operating or performing any installation or removal of optional modules and
accessories. The Symbol Definitions are on pages 2 and 13 of this manual.
Follow all safety precautions before, during, and after any treatment.
Read, understand and follow the indications, contraindications, and adverse effects of the modalities associated with this system found
on pages 7 through 9 of this manual before administering any treatment.
Keep informed of appropriate indications and contraindications for the use of all modalities utilized with this Therapy System.
This system, optional modules, and accessories are to be used and sold only under the prescription and supervision of a physician or
licensed practitioner.

DISCONNECT THE SYSTEM FROM THE POWER SOURCE (OUTLET OR


REMOVE BATTERY MODULE IF INSTALLED) BEFORE ATTEMPTING
ANY MAINTENANCE, INSTALLATION, REMOVAL, OR REPLACEMENT
PROCEDURES TO PREVENT ELECTRICAL SHOCK AND POSSIBLE
DAMAGE TO SYSTEM.

95

INSTALLATION/REMOVAL

Intelect Advanced Therapy System

INSTALLATION CHANNEL 3/4 ELECTROTHERAPY MODULE (continued)


Nomenclature

1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.

6
1

Also Included:
Four 4 mm X 20 mm mounting screws
Channel 3 and 4 Lead Wires
Patient Interrupt Switch (Ch 3/4)
Carbon Electrodes
Electrode Sponges
Sample of Dura-Stick II electrodes
Nylatex Wraps
9

Channel 3/4 Electrotherapy Module


Extended Front Access Panel
Module to System Mounting Holes
Module to System Feet Alignment Indents
Power Cord Routing Port
Module to System Connector
Operator Remote Control Connector*
Patient Interrupt Switch Connector*
Channel 3 Lead Wire Connector*
Channel 4 Lead Wire Connector*
Microcurrent Probe Connector*

11
10

* Refer to page 13 for Symbol Definitions.


96

INSTALLATION/REMOVAL

Intelect Advanced Therapy System

INSTALLATION CHANNEL 3/4 ELECTROTHERAPY MODULE (continued)


Specifications

DIMENSIONS
Width . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 cm (8.250")
Depth . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .30 cm (11.875")
Height . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11.5 cm (4.500")
WEIGHT
Standard Weight. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .50 kg (1.0 lbs)

HEIGHT

POWER
Input . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .System Dependent
Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .System Dependent

DEPTH

Electrical Class . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .CLASS I


Electrical Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . TYPE BF
WIDTH

Regulatory Compliance
UL/IEC/EN 60601-1
IEC 60601-2-10

NOTE:
All waveforms except High Voltage Pulsed Current (HVPC) of the
Intelect Advanced Therapy System have been designed with a
200 mA current limit.
VMS, VMS Burst and all TENS waveform output intensities are
measured, specified and listed to peak, not peak to peak.

0413

Waveform & Current Specifications


All waveform/currents available to the Intelect Advanced Therapy
System are available to the Channel 3/4 Electrotherapy Module
once installation is complete. Refer to pages 16 through 25 for
available waveform specifications.
97

INSTALLATION/REMOVAL

Intelect Advanced Therapy System

INSTALLATION CHANNEL 3/4 ELECTROTHERAPY MODULE (continued)


Disconnect Mains Power
Remove Lead Wires and Accessories
Remove the Front Access Cover and
disconnect the Lead Wires and Accessories
from the Therapy System.
DISCONNECT THE SYSTEM FROM THE
POWER SOURCE (OUTLET OR REMOVE
BATTERY MODULE IF INSTALLED) BEFORE
ATTEMPTING ANY MAINTENANCE,
INSTALLATION, REMOVAL, OR REPLACEMENT
PROCEDURES TO PREVENT ELECTRICAL
SHOCK AND POSSIBLE DAMAGE TO SYSTEM.

REMOVE LEAD
WIRES AND
ACCESSORIES

Remove Therapy System from Cart


Remove the Therapy System from the
Therapy System Cart, if equipped. Refer to
the Therapy System Cart User Manual for
proper instructions.
Place Therapy System face down on a clean
working surface protected with a soft, clean
fabric to prevent damage to the lens.
SEMG
MODULE

Disconnect the Mains Power Cord from


the power supply. Remove the Rear Access
Panel and disconnect the Mains Power
Cord from the Therapy System.
REAR
ACCESS
PANEL
MAINS
POWER
CORD

LANYARD

NOTE:
Do not remove the sEMG Module, if
installed. The sEMG Module will not
interfere with installation of the Channel
3/4 Electrotherapy Module.
98

INSTALLATION/REMOVAL

Intelect Advanced Therapy System

INSTALLATION CHANNEL 3/4 ELECTROTHERAPY MODULE (continued)


Release Ribbon Cable
Position Therapy System and Module
Position Therapy System and the Channel
Remove and discard the vinyl label holding
3/4 Electrotherapy Module as shown.
the Ribbon Cable in the cavity on the
Therapy System.
Carefully unroll the Ribbon Cable, making
certain not to disconnect it from the
Therapy System.

Connect Ribbon Cable


Carefully align the Ribbon Cable Connector
to the Module Connector Pins and press
down to connect.

CAREFULLY UNROLL
RIBBON CABLE

RIBBON CABLE MUST BE AS SHOWN!


Make certain Ribbon Cable is completely
seated to Module Connector Pins.
99

INSTALLATION/REMOVAL

Intelect Advanced Therapy System

INSTALLATION CHANNEL 3/4 ELECTROTHERAPY MODULE (continued)

Do not twist Ribbon Cable. If power is


applied to the system with misalignment of
pins or a twisted ribbon cable, the controlling
electronics in the Module will be destroyed
and possible damage to the System's internal
components could occur.

Secure Therapy System to Module

Front Access Panel

Carefully place the Therapy System and


Module on one side. With a #1 Phillips
Screwdriver, install the four 4 mm x 20 mm
screws.
Tighten screws until the Module does not
move on the Therapy System.

With a #1 Phillips Screwdriver, remove the


screw retaining the existing Front Access
Panel.
Install Lanyard to the new Extended Front
Access Panel using the same screw.

Set Therapy System onto Module


Set the Therapy System on the Module.
Make certain the Feet of the Therapy
System are resting in the Module Indents.

100

INSTALLATION/REMOVAL

Intelect Advanced Therapy System

INSTALLATION CHANNEL 3/4 ELECTROTHERAPY MODULE (continued)


Install Lead Wires and Accessories
Install Lead Wires and additional accessories
to Front Panel. Refer to page 13 for Symbol
Definitions.

Install Front Access Panel


Install the new Extended Front Access Panel
onto Therapy System.
Make certain Lanyard does not become
kinked.
LANYARD

Connect Mains Power


Connect the Mains Power Cord to the
Therapy System.
Install Rear Access Panel.
Connect the Mains Power Cord to an
approved power source.
REAR
ACCESS
PANEL
MAINS
POWER
CORD

Mount to Therapy System Cart


If mounting Therapy System to a Therapy
System Cart, refer to Therapy System Cart
User Manual for instructions.

101

INSTALLATION/REMOVAL

Intelect Advanced Therapy System

INSTALLATION CHANNEL 3/4 ELECTROTHERAPY MODULE (continued)


Turn Therapy System On
Turn the System On using the On/Off
Switch. The System will automatically
recognize the added Module and display a
configuration change message.
Read and carefully follow the instructions
on the screen.

Verify that the Module installed is the Module


displayed in the message BEFORE pressing
the START button. If it is not, DO NOT press
the START button. Turn the System OFF
and back ON. If the problem continues, call
the selling dealer or Chattanooga Group
Technical Support immediately.
DO NOT USE THE SYSTEM until all necessary
repairs are made by a Technician certified
by Chattanooga Group. If use is attempted
before repairs are made, the System may
operate unpredictably and has the potential
of causing injury to the patient or damage to
the System's internal components.

102

INSTALLATION/REMOVAL

Intelect Advanced Therapy System

REMOVAL CHANNEL 3/4 ELECTROTHERAPY MODULE


Disconnect Mains Power

DISCONNECT THE SYSTEM FROM THE POWER


SOURCE (OUTLET OR REMOVE BATTERY
MODULE IF INSTALLED) BEFORE ATTEMPTING
ANY MAINTENANCE, INSTALLATION,
REMOVAL, OR REPLACEMENT PROCEDURES
TO PREVENT ELECTRICAL SHOCK AND
POSSIBLE DAMAGE TO SYSTEM.

Remove Therapy System from Cart


Remove the Therapy System from the
Therapy System Cart, if equipped. Refer to
the Therapy System Cart User Manual for
proper instructions.
Place Therapy System face down on a clean
working surface protected with a soft, clean
fabric to prevent damage to the lens.

Remove Lead Wires and Accessories


Remove the Front Access Cover and
disconnect the Lead Wires and Accessories
from the Therapy System and Channel 3/4
Electrotherapy Module.

REMOVE LEAD
WIRES AND
ACCESSORIES

Disconnect the Mains Power Cord from


the power supply. Remove the Rear Access
Panel and disconnect the Mains Power
Cord from the Therapy System.
REAR
ACCESS
PANEL

NOTE:
Keep Lead Wires and accessories for later
re-installation to the Therapy System.

MAINS
POWER
CORD

NOTE:
It is not necessary to remove the
sEMG Module from the Channel 3/4
Electrotherapy Module, if installed.
103

INSTALLATION/REMOVAL

Intelect Advanced Therapy System

REMOVAL CHANNEL 3/4 ELECTROTHERAPY MODULE (continued)


Remove Screws Securing Module

Disconnect Ribbon Cable at Module

Store and Secure Ribbon Cable

With a #1 Phillips Screwdriver, remove the


four 4 mm x 20 mm screws securing the
Module to the Therapy System.

Separate the Module from the Therapy


System and disconnect the Ribbon Cable
from the Module Connector Pins.

Roll the Ribbon Cable up and store in


the cavity of the Therapy System. Secure
Ribbon Cable with a nonpermanent
adhesive tape.

Do not disconnect Ribbon Cable from


the Therapy System.
DISCONNECT
RIBBON FROM
MODULE ONLY

104

INSTALLATION/REMOVAL

Intelect Advanced Therapy System

REMOVAL CHANNEL 3/4 ELECTROTHERAPY MODULE (continued)


Front Access Panel
Install Lead Wires and Accessories
Re-install Lead Wires and Accessories to the
With a #1 Phillips Screwdriver, remove the
Therapy System Front Panel.
screw retaining the existing Front Access
Panel.
Install Lanyard to the original Front Access
LANYARD
Panel using the same screw.

Connect Mains Power


Connect the Mains Power Cord to the
Therapy System.
Install Rear Access Panel.
Connect the Mains Power Cord to an
approved power source.
REAR
ACCESS
PANEL
MAINS
POWER
CORD

NOTE:
When re-installing the Front Access Panel
to the Therapy System, make certain the
Lanyard does not become kinked.

105

INSTALLATION/REMOVAL

Intelect Advanced Therapy System

CHANNEL 3/4 ELECTROTHERAPY MODULE REMOVAL (continued)


Turn Therapy System On
Turn the System On using the On/Off
Switch. The System will automatically
recognize the Module has been removed
and will display a configuration change
message.
Read and carefully follow the instructions
on the screen.

Verify that the Module installed is the Module


displayed in the message BEFORE pressing
the START button. If it is not, DO NOT press
the START button. Turn the System OFF
and back ON. If the problem continues, call
the selling dealer or Chattanooga Group
Technical Support immediately.
DO NOT USE THE SYSTEM until all necessary
repairs are made by a Technician certified
by Chattanooga Group. If use is attempted
before repairs are made, the System may
operate unpredictably and has the potential
of causing injury to the patient or damage to
the System's internal components.

106

TROUBLESHOOTING

Intelect Advanced Therapy System

ERROR CODES
General Information
The Intelect Advanced Therapy Systems incorporate error messages, and warnings to inform the user of problems or potential problems
with the system, modality, or accessories. These are numbered so the user can possibly correct the problem without the aid of service
personnel. Use the following Troubleshooting Charts to define the error codes, and locate the probable cause and possible remedies
before contacting the dealer or factory for technical service.
Code
Number

Type
Message

Probable Cause

Possible Remedies

100

Warning

Overcurrent

A. Check Electrodes and Lead Wires. Make certain Lead Wires are not damaged and are
properly connected to the system. Make certain Lead Wires are properly connected to
the Electrodes and that electrodes are not damaged and are making proper contact with
treatment area.
B. Replace Lead Wires and Electrodes.

101

Warning

Shorted Lead Wires

A. Check Electrodes and Lead Wires. Make certain Lead Wires are not damaged and are properly
connected to the system. Make certain Lead Wires are properly connected to the Electrodes
and that electrodes are not damaged and are making proper contact with treatment area.
B. Replace Lead Wires and Electrodes.

102

Warning

Bad Contact Quality

A. Make certain Electrodes are making proper contact with the treatment area.
B. Make certain Lead Wires are properly connected to Electrodes.
C. Replace Electrodes and Lead Wires.

103

Warning

Blank Patient ID

Properly enter Patient ID. Refer to Therapy System User Manual for Patient Data Card instructions.

104

Warning

1. Blank Protocol Name


2. Blank Sequence Name

Properly enter Protocol or Sequence Name. Refer to the appropriate section of the Therapy System
User Manual.

106
107

Warning
Warning

1. Attempting to delete factory set Sequence.


2. Attempting to delete Clinical Protocol.

Cannot delete factory set Clinical Protocols or factory set Sequences.

107

TROUBLESHOOTING

Intelect Advanced Therapy System

ERROR CODES (continued)


Code
Number

Type
Message

Probable Cause

Possible Remedies

108

Warning

Attempting to save additional User Protocols or Sequences after


system memory has reached the maximum allowed (200).

Delete some User Protocols or Sequences. Refer to appropriate section of the Therapy System User
Manual for instructions.

109
110
111

Warning
Warning
Warning

Attempting to access protocols or sequences and none are found


in the system.

A. User Protocols- No protocols have been saved in the system. Refer to Therapy System User
Manual to save User Protocols.
B. Sequences- No User Sequences have been saved in the system. Refer to Therapy System User
Manual to save Sequences.

112

Warning

Ultrasound Applicator disconnected from system during treatment


session.

A. Connect Ultrasound Applicator to system.


B. If Ultrasound Applicator is connected, reset system by turning power switch Off and On.
C. If problem persists, connect a known good Ultrasound Applicator. If problem continues,
contact dealer or Chattanooga Group for service.

113

Warning

Attempting to perform Ultrasound treatment with no Applicator


connected to the system.

A. Connect the desired Ultrasound Applicator to the system.


B. If Ultrasound Applicator is connected, reset system by turning power switch Off and On.
C. If problem persists, connect a known good Ultrasound Applicator. If problem continues,
contact dealer or Chattanooga Group for service.

114

Warning

Ultrasound Applicator is not calibrated.

Attempt to use a known good Applicator. If problem continues, contact dealer or Chattanooga
Group for service.

115

Warning

Ultrasound Applicator is too hot.

Allow Ultrasound Applicator Sound Head to cool to ambient temperature.

116
117

Warning
Warning

1. No Patient Data Card is inserted into the system.


2. Attempted to use an Invalid Patient Data Card.

A. Properly insert the Patient Data Card into the system port. Refer to Therapy System User
Manual for new and existing Patient Data Card instructions.
B. Attempt to use a known good Patient Data Card.
C. Make certain a Patient Data Card and not an sEMG Data Card is being used.
D. If problem continues, contact dealer or Chattanooga Group for service.

108

TROUBLESHOOTING

Intelect Advanced Therapy System

ERROR CODES (continued)


Code
Number

Type
Message

Probable Cause

Possible Remedies

118

Warning

Attempting to save additional User Protocols or Sequences after


system memory has reached the maximum allowed (200).

Delete some User Protocols or Sequences. Refer to appropriate section of the Therapy System User
Manual for instructions.

119
120
121
122

Warning
Warning
Warning
Warning

1. Attempted to read a treatment from Patient Data Card that is


not a valid treatment for the system
2. Attempted to use a Non-Patient Data Card.
3. No Patient Data Card inserted into system port.
4. Unknown type of smart card inserted into system.

A. Use a Patient Data Card with proper treatment data for the system.
B. Properly insert a Patient Data Card.
C. Insert a known good Patient Data Card.
D. If problem persists, insert a known good Patient Data Card. If problem continues, contact
dealer or Chattanooga Group for service.

123

Warning

Patient Data Card is full.

Erase Patient Data Card. Refer to Therapy System User Manual for instructions.

124

Warning

Patient Treatment Data already saved.

A. Cannot save same data again on Patient Data Card.


B. Use a new Patient Data Card to resave data.
C. Erase Patient Data Card and resave treatment data.

125

Warning

Multimedia Card (MMC) not in system port.

A. Properly insert the MMC card into the system port.


B. Insert a known good MMC Card. If problem continues, contact dealer or Chattanooga Group
for service.

126

Warning

No valid channels are available for attempted treatment.

A. Complete existing treatment before attempting to start another.


B. Reset Therapy System by turning main power switch Off and On.

127
128

Warning
Warning

1. No sEMG Channels are available for treatment.


2. No sEMG Module installed or detected by system.

A. Wait until current treatment is complete.


B. Reset Therapy System by turning main power switch Off and On.
C. Make certain sEMG Module is properly installed. Refer to sEMG Module User Manual for
installation instructions.
D. Replace sEMG Module with known good sEMG Module.
E. If problem continues, contact dealer or Chattanooga Group for service.

109

TROUBLESHOOTING

Intelect Advanced Therapy System

ERROR CODES (continued)


Code
Number

Type
Message

Probable Cause

Possible Remedies

129

Warning

sEMG Data Card full.

sEMG Data Card faulty. Insert a known good sEMG Data Card. If problem continues, contact dealer
or Chattanooga Group for service.

130

Warning

Another treatment is running while attempting to set up and


perform a Laser Therapy treatment.

A. Allow existing treatment to complete before starting Laser Therapy.


B. If no other treatment is running, reset Therapy System by turning main power switch
Off and On.

131

Warning

Treatment Room Door Lockout is breached.

A. Make certain Treatment Room Door is completely closed.


B. Make certain the Lockout cable is connected to the system.
C. Replace Lockout to System cable with a known good cable.
D. Contact department responsible for installation of the Treatment Room Door Lockout
mechanism for maintenance or repair.
E. If problem continues, send Laser Module to Factory for service.

132

Warning

Attempted to start a laser treatment but no Laser Applicator is


plugged in.

A. Connect desired Laser Applicator to the system.


B. If Applicator is connected, reset Therapy System by turning main power switch Off and On.
C. Connect a known good Laser Applicator.
D. If problem continues, send Laser Module to Factory for service.

133

Warning

Laser Applicator became unplugged while performing a laser


treatment.

A. Connect desired Laser Applicator to the system.


B. If Laser Applicator is connected, reset Therapy System by turning main power switch
Off and On.
C. Connect a known good Laser Applicator.
D. If problem continues, send Laser Module to Factory for service.

134

Warning

Entered incorrect laser PIN.

A. Enter correct Laser PIN number.


B. If problem continues, send Laser Module to Factory for service.

110

TROUBLESHOOTING

Intelect Advanced Therapy System

ERROR CODES (continued)


Code
Number

Type
Message

Probable Cause

Possible Remedies

135

Warning

Control Board Software upgrade warning.

Upgrade Control Board Software to latest version. Contact dealer or Chattanooga Group for latest
software upgrade and instructions.

136

Warning

Stim Board Main Software upgrade warning.

Upgrade Stim Board Software to latest version. Contact dealer or Chattanooga Group for latest
software upgrade and instructions.

137

Warning

Stim Board Main Software upgrade warning.

Upgrade Stim Board Software to latest version. Contact dealer or Chattanooga Group for latest
software upgrade and instructions.

138

Warning

Ultrasound Board Software upgrade warning.

Upgrade Ultrasound Board Software to latest version. Contact dealer or Chattanooga Group for
latest software upgrade and instructions.

139

Warning

Laser Board Software upgrade warning.

Upgrade Laser Board Software to latest version. Contact dealer or Chattanooga Group for latest
software upgrade and instructions.

140

Warning

MMC Software upgrade warning.

Upgrade MMC Software to latest version. Contact dealer or Chattanooga Group for latest software
upgrade and instructions.

141

Warning

Battery Module Software upgrade warning.

Upgrade Battery Software to latest version. Contact dealer or Chattanooga Group for latest
software upgrade and instructions.

142

Warning

A Laser Protocol was selected, but no Laser Module is installed


on system.

Install Laser Module to Therapy System. Refer to Laser Module User Manual for installation
Instructions.

143

Warning

A Laser Protocol was selected, but no Laser Applicator connected


to system.

A. Connect proper Laser Applicator to the system.


B. If Laser Applicator is connected, reset Therapy System by turning main power switch
Off and On.
C. Connect a known good Laser Applicator.
D. If problem continues, send Laser Module to Factory for service.

111

TROUBLESHOOTING

Intelect Advanced Therapy System

ERROR CODES (continued)


Code
Number

Type
Message

Probable Cause

Possible Remedies

144

Warning

Wrong Laser Applicator connected to system for the protocol


selected.

A. Connect correct Laser Applicator to the system.


B. If Applicator is connected, reset Therapy System by turning main power switch Off and On.
C. Connect a known good Laser Applicator.
D. If problem continues, send Laser Module to Factory for service.

145

Warning

Patient Data Card button on Home screen was pressed with no


Patient Data Card installed into system port and no treatment
currently being performed.

Properly insert a Patient Data Card, set up and perform the treatment and save data to Patient
Data Card.

In the event that an Error message or Warning appears beginning


with a 2 or 3, immediately stop all use of the system and contact the
dealer or Chattanooga Group for service. Errors and Warnings in these
categories indicate an internal problem with the system that must be
tested by Chattanooga Group or a Field Service Technician certified by
Chattanooga Group before any further operation or use of the system.
Use of a system that indicates an Error or Warning in these categories
may pose a risk of injury to the patient, user, or extensive internal damage
to the system.

112

MAINTENANCE

Intelect Advanced Therapy System

CARING FOR THE THERAPY SYSTEM


Cleaning the Therapy System
With the system disconnected from the power source, clean the
system with a clean, lint free cloth moistened with water and mild
antibacterial soap. If a more sterile cleaning is needed, use a cloth
moistened with an antimicrobial cleaner.
Do not submerse the system in liquids. Should the unit
accidentally become submersed, contact the dealer or
Chattanooga Group Service Department immediately. Do not
attempt to use a system that has been wet inside until inspected
and tested by a Service Technician Certified by Chattanooga Group.

FACTORY SERVICE
When the Intelect Advanced Therapy System or any of the
accessory modules require factory service, contact the selling dealer
or Chattanooga Group Service Department.
All Therapy System and accessory modules returned to the factory for
service must include the following;
WARRANTY REPAIR/OUT OF WARRANTY REPAIR
1. Written statement containing the following information;
RA Number- Obtain from Factory
Therapy System or Module Model Number
Therapy System or Module Serial Number
Contact Person with Phone and Fax Numbers
Billing Address (for Out of Warranty Repair)
Shipping Address (Where to Ship Unit after Repair)
Detailed Description of Problem or Symptoms
2. Copy of original invoice issued at purchase of the Therapy System
or Module.
3. Ship the unit to address specified by an authorized service
technician.
Service to these units should be performed only by Service
Technicians certified by Chattanooga Group.
Ultrasound Applicators require annual calibration, from the date
placed in service, by the Factory or a Service Technician certified by
Chattanooga Group.

Do not allow liquids to enter the ventilation holes in the optional


modules. This could permanently damage the modules.
Cleaning Electrode Sponges
Thoroughly clean spnges after each use with medical grade alcohol.

Cleaning the Lens


Clean the Therapy System Screen Lens using NOVUS Polish System.
Contact Novus at: www.novuspolish.com
CALIBRATION REQUIREMENTS
Calibrating Ultrasound Applicators
Annual factory calibration is required for all Ultrasound Applicators.
Only the Applicators should be sent to the factory or a Field
Technician certified by Chattanooga Group for this procedure.
NOVUS is the Registered Trademark of NOVUS Inc.

113

WARRANTY

Intelect Advanced Therapy System

Chattanooga Group ("Company") warrants that the Intelect Advanced Therapy System ("Product") is free of defects in material and workmanship. This warranty shall remain in
effect for two years (24 months) from the date of original consumer purchase. If this Product fails to function during the two year warranty period due to a defect in material
or workmanship, Company or the selling dealer will repair or replace this Product without charge within a period of thirty (30) days from the date on which the Product is
returned to the Company or the dealer.
All repairs to the Product must be performed by a service center authorized by the Company. Any modifications or repairs performed by unauthorized centers or groups will
void this warranty.
The warranty period for accessories is 180 days. Accessories include Lead Wires, Electrodes, and Nylatex.
This warranty does not cover:
Replacement parts or labor furnished by anyone other than the Company, the selling dealer, or a service technician certified by the Company.
Defects or damage caused by labor furnished by someone other than Company, the selling dealer, or a certified Company service technician.
Any malfunction or failure in the Product caused by product misuse, including, but not limited to, the failure to provide reasonable and required maintenance or any use that
is inconsistent with the Product User's Manual.
COMPANY SHALL NOT BE LIABLE IN ANY EVENT FOR INCIDENTAL OR CONSEQUENTIAL DAMAGES.
Some locations do not allow the exclusion or limitation of incidental or consequential damages, so the above limitation or exclusion may not apply to you.
To obtain service from Company or the selling dealer under this warranty:
1. A written claim must be made within the warranty period to the Company or the selling dealer. Written claims made to the Company should be sent to:
Chattanooga Group
4717 Adams Road
Hixson, TN 37343 USA
Phone: +1-423-870-7200
FAX: +1-423-870-2046
and
2. The Product must be returned to the Company or the selling dealer by the owner.
This warranty gives you specific legal rights and you may also have other rights which vary from location to location.
The Company does not authorize any person or representative to create for it any other obligation or liability in connection with the sale of the Product.
Any representation or agreement not contained in the warranty shall be void and of no effect.
THE FOREGOING WARRANTY IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESSED OR IMPLIED,
INCLUDING ANY WARRANTY OR MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE.

114

ISO 13485 CERTIFIED

4717 Adams Road


P.O. Box 489
Hixson, TN 37343 U.S.A.
+1-423-870-7200 OUTSIDE U.S.A
+1 423-870-2046 OUTSIDE U.S.A. FAX
www.chattgroup.com

27429C
2005 Encore Medical, L.P.

0413